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S.No.

Dosage Form

Generic Name

Details

B-Complex with L-Lysine Syrup (For therapeutic use)

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Thiamine Hydrochloride	I.P.	2 mg
Riboflavine Sodium Phosphate	I.P.	2.5 mg
Pyridoxine Hydrochloride	I.P.	0.75 mg
Nicotinamide	I.P.	15 mg
D-Panthenol	I.P.	3 mg
Cyanocobalamin	I.P.	2 mcg
Lysine Hydrochloride	I.P.	375 mg
Zinc Gluconate (eq. to elemental Zinc)	USP	5 mg
Sorbitol Solution 70% (Non-crystallizing)	I.P.	q.s.
In a flavoured syrupy base		q.s.
Excipients		q.s.
Colour: Approved colour used

Dextromethorphan Hydrobromide, Chlorpheniramine Maleate Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Dextromethorphan Hydrobromide	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	2 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved Colour used

Dextromethorphan Hydrobromide, Chlorpheniramine Maleate and Phenylepherine Hydrochloride Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Dextromethorphan Hydrobromide	I.P.	15 mg
Chlorpheniramine Maleate	I.P.	2 mg
Phenylepherine Hydrochloride	I.P.	5 mg
Excipients		q.s.
In a palatable sugar-free base		q.s.
Approved Colour used

Domperidone Oral Drop

Composition	Standard	Quantity (per 1 ml)
Each 1 ml contains :
Domperidone	I.P.	10 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved Colour used

Ambroxol HCl, Dextromethorphan HBR, Phenylepherine HCl, Chlorpheniramine Maleate and Menthol Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ambroxol Hydrochloride	I.P.	15 mg
Dextromethorphan Hydrobromide	I.P.	10 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	2 mg
Menthol	I.P.	1.5 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Dried Aluminium Hydroxide Gel, Oxetacaine and Magnesium Hydroxide Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Aluminium Hydroxide (added as Dried Aluminium Hydroxide Gel 380 mg)	I.P.	0.291 gm
Oxetacaine	B.P.	10 mg
Magnesium Hydroxide (as Magnesium Hydroxide Paste)	I.P.	98 mg
Excipients		q.s.
In a flavoured palatable base		q.s.
Approved colour used

Levosalbutamol Sulphate, Ambroxol Hydrochloride, and Guaiphenesin Oral Drops

Composition	Standard	Quantity (per 1 ml)
Each 1 ml contains :
Levosalbutamol Sulphate (eq. to Levosalbutamol)	I.P.	0.25 mg
Ambroxol Hydrochloride	I.P.	7.5 mg
Guaiphenesin	I.P.	12.5 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved Colour used

Cyproheptadine Hydrochloride and Tricholine Citrate Drops

Composition	Standard	Quantity (per 1 ml)
Each 1 ml contains :
Cyproheptadine Hydrochloride	I.P.	2 mg
Tricholine Citrate (65%)		55 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved Colour used

Ursodeoxycholic Acid Suspension 250mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ursodeoxycholic Acid	I.P.	250 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Ursodeoxycholic Acid Suspension 125mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ursodeoxycholic Acid	I.P.	125 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Paracetamol, Phenylephrine HCl, Chlorpheniramine Maleate, Sodium Citrate and Menthol syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	125 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	0.5 mg
Sodium Citrate	I.P.	60 mg
Menthol	I.P.	1 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Milk of Magnesia, Liquid Paraffin and Sodium Picosulfate oral emulsion

Composition	Standard	Quantity (per 5 ml)
Each 5 ml (1 teaspoonful approx.) contains :
Milk of Magnesia	I.P.	3.75 ml
Liquid Paraffin	I.P.	1.25 ml
Sodium Picosulfate	B.P.	3.33 mg
Excipients		q.s.
Indication		For symptomatic treatment of constipation in adults
Dosage		As directed by the physician
Approved colour used

Ferric Ammonium Citrate, Folic acid and Vitamin B12 Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ferric Ammonium Citrate (eq. to Elemental Iron)	I.P.	160 mg (Elemental Iron 32.80 mg)
Folic Acid	I.P.	0.5 mg
Cyanocobalamin	I.P.	7.5 mcg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Colour		Approved colour used

Ofloxacin & Metronidazole Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ofloxacin	I.P.	100 mg
Metronidazole Benzoate (eq. to Metronidazole)	I.P.	200 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Azithromycin Oral Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Azithromycin (as dehydrate) eq. to Azithromycin anhydrous	I.P.	100 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Dill Oil, Fennel Oil with Simethicone Oral Drops

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Dill Oil	B.P.	0.005 ml
Fennel Oil	USP	0.0007 ml
Simethicone Emulsion (30%) eq. to Simethicone	USP	40 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Zinc Gluconate Oral Solution

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Zinc Gluconate (eq. to elemental Zinc)	B.P.	20 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Paracetamol Suspension I.P. 500 mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	500 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Levetiracetam Oral Solutions I.P 500mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Levetiracetam	I.P.	500 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Ambroxol Hydrochloride Syrup 30mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ambroxol Hydrochloride	I.P.	30 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Ranitidine Oral Solution I.P

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ranitidine Hydrochloride (eq. to Ranitidine)	I.P.	75 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Ibuprofen and Paracetamol Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ibuprofen	I.P.	100 mg
Paracetamol	I.P.	162.5 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Hydroxyzine Oral Solution I.P.

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Hydroxyzine Hydrochloride	I.P.	10 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Paracetamol, Phenylephrine HCl, Chlorpheniramine Maleate, Sodium Citrate and Menthol Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	125 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	0.5 mg
Sodium Citrate	I.P.	60 mg
Menthol	I.P.	1 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Fexofenadine Hydrochloride Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Fexofenadine Hydrochloride	I.P.	60 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Fexofenadine Hydrochloride Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Fexofenadine Hydrochloride	I.P.	30 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Phenylepherine Hydrochloride & Chlorpheniramine Maleate Syrup I.P

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Phenylephrine Hydrochloride	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	2 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Iron, Vitamin B12 and Folic Acid Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ferric Ammonium Citrate (eq. to elemental Iron)	I.P.	110.55 mg
Folic Acid	I.P.	1.5 mg
Cyanocobalamin	I.P.	15 mcg
In a flavoured syrupy base		q.s.
Excipients		q.s.
Colour: Approved colour used

Pyridoxine Hydrochloride, Nicotinamide, Cyanocobalamin and Lysine Hydrochloride Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Pyridoxine Hydrochloride	I.P.	0.75 mg
Nicotinamide	I.P.	15 mg
Cyanocobalamin	I.P.	2 mcg
Lysine Hydrochloride	I.P.	37.5 mg
In a flavoured syrupy base		q.s.
Excipients		q.s.
Colour: Approved colour used

Liquid Paraffin & Milk of Magnesia Suspension

Composition	Standard	Quantity (per 15 ml)
Each 15 ml contains :
Liquid Paraffin	I.P.	3.75 ml
Milk of Magnesia	I.P.	11.25 ml
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved colour used

Promethazine Syrup I.P

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Promethazine Hydrochloride	I.P.	5 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved colour used

Levocetirizine Dihydrochloride Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Levocetirizine Dihydrochloride	I.P.	2.5 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved colour used

Levodropropizine & Chlorpheniramine Maleate Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Levodropropizine	I.P.	30 mg
Chlorpheniramine Maleate	I.P.	2 mg
Excipients		q.s.
Approved Colour used

Diphenhydramine HCl, Ammonium Chloride, Sodium Citrate and Menthol Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Diphenhydramine Hydrochloride	I.P.	14.08 mg
Ammonium Chloride	I.P.	138 mg
Sodium Citrate	I.P.	57.03 mg
Menthol	I.P.	1.14 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Potassium Citrate, Magnesium Citrate & Pyridoxine HCl Oral Solution

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Potassium Citrate	I.P.	1100 mg
Magnesium Citrate	USP	375 mg
Pyridoxine Hydrochloride	I.P.	20 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Calcium, Magnesium, Zinc & Vitamin D3 Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Calcium Carbonate (eq. to elemental Calcium)	I.P.	625 mg
Magnesium Hydroxide (eq. to elemental Magnesium)	I.P.	75 mg
Zinc Gluconate (eq. to elemental Zinc)	USP	2 mg
Vitamin D3	I.P.	200 I.U.
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Sodium Alginate, Sodium Bicarbonate and Calcium Carbonate Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Sodium Alginate	I.P.	250 mg
Sodium Bicarbonate	I.P.	133.5 mg
Calcium Carbonate	I.P.	80 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Dried Aluminium Hydroxide, Magnesium Hydroxide, Simethicone Suspension

Composition	Standard	Quantity (per 10 ml)
Each 10 ml contains :
Dried Aluminium Hydroxide	I.P.	250 mg
Magnesium Hydroxide	I.P.	250 mg
Simethicone	I.P.	50 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Chlorhexidine Gluconate Mouth Wash IP

Composition	Standard	Quantity
Chlorhexidine Gluconate	I.P.	0.2% w/v
In a pleasantly flavoured syrupy base		q.s.
Approved colour used

Paracetamol, Cetirizine HCl, Phenylephrine HCl and Menthol Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	250 mg
Cetirizine Hydrochloride	I.P.	2.5 mg
Phenylephrine Hydrochloride	I.P.	2.5 mg
Menthol	I.P.	1 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved colour used

Cetirizine HCl, Phenylephrine HCl and Paracetamol Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Cetirizine Hydrochloride	I.P.	2.5 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Paracetamol	I.P.	125 mg
Excipients		q.s.
In a flavoured syrupy base		q.s.
Approved colour used

Levocloperastine Fendizoate Oral Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Levocloperastine Fendizoate (eq. to Levocloperastine Hydrochloride)		20 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Paracetamol, Phenylephrine & Chlorpheniramine Maleate Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	250 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	2 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Fungal Diastase and Pepsin Syrup

Composition	Standard	Quantity (per 15 ml)
Each 15 ml contains :
Fungal Diastase (1:1200) (Derived from Aspergillus oryzae, digest not less than 60 gm of cooked starch)	I.P.	50 mg
Pepsin (1:3000) (Digest not less than 60 gm of coagulated egg albumin)	I.P.	10 mg
Excipients		q.s.
In a Flavoured Palatable base		q.s.
Approved Colour used
Dosage: Adult: One teaspoonful immediately after the meal. Children: Half the adult dose. As directed by the physician.

Sucralfate and Oxetacaine Suspension

Composition	Standard	Quantity (per 10 ml)
Each 10 ml contains :
Sucralfate	USP	1000 mg
Oxetacaine	B.P.	20 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Lactulose Oral Solution U.S.P.

Composition	Standard	Quantity (per 15 ml)
Each 15 ml contains :
Lactulose Concentrate (eq. to Lactulose 66% w/v)	USP	10 gm
In a flavoured syrup base		q.s.
Excipients		q.s.
Approved colour used

Mefenamic Acid and Paracetamol Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Mefenamic Acid	I.P.	100 mg
Paracetamol	I.P.	250 mg
In Flavoured syrup base		q.s.
Approved colour used

Di-Sodium Hydrogen Citrate Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Di-Sodium Hydrogen Citrate	B.P.	1.37 gm
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Ofloxacin, Metronidazole Benzoate and Simethicone Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ofloxacin	I.P.	50 mg
Metronidazole Benzoate (eq. to Metronidazole)	I.P.	120 mg
Simethicone	I.P.	10 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Sodium Picosulfate Oral Solution B.P.

Composition	Standard	Quantity (per 5 ml)
Each 5 ml (1 teaspoonful approx.) contains :
Sodium Picosulfate	B.P.	5 mg
Excipients		q.s.
Dosage: As directed by the physician. Approved Colour used

Milk of Magnesia, Liquid Paraffin and Sodium Picosulfate oral emulsion

Composition	Standard	Quantity (per 5 ml)
Each 5 ml (1 teaspoonful approx.) contains :
Sodium Picosulfate	B.P.	33.3 mg
Liquid Paraffin	I.P.	1.25 ml
Milk of Magnesia	I.P.	3.75 ml
Excipients		q.s.
Indication: For symptomatic treatment of constipation in adults. Dosage: As directed by the physician. Approved Colour used

Dried Aluminium Hydroxide, Magnesium Hydroxide, Simethicone and Oxetacaine Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Dried Aluminium Hydroxide Gel (eq. to Aluminium Hydroxide)	I.P.	600 mg
Magnesium Hydroxide	I.P.	300 mg
Simethicone	I.P.	25 mg
Oxetacaine	B.P.	10 mg
Purified Water	I.P.	q.s.
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Ofloxacin Oral Suspension I.P. 100mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ofloxacin	I.P.	100 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Ondansetron Oral Solution I.P. 2 mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ondansetron Hydrochloride (eq. to Ondansetron)	I.P.	2 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Paracetamol Paediatric Oral Suspension I.P. 250mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	250 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Paracetamol Paediatric Oral Suspension I.P. 125mg

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Paracetamol	I.P.	125 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Magaldrate and Simethicone Oral Suspension I.P.

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Magaldrate (Anhydrous)	I.P.	400 mg
Simethicone	I.P.	60 mg
In a suspension base
Excipients		q.s.
Approved Colour used

Mefenamic Acid and Paracetamol Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Mefenamic Acid	I.P.	50 mg
Paracetamol	I.P.	125 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Vitamin D3 oral Solution 60000 I.U (Nano Shot)

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Cholecalciferol (Vitamin D3) (In nano droplet form)	I.P.	60,000 I.U.
In a flavoured sorbitol base		q.s.
Colour: Tartrazine Supra

Ambroxol Hydrochloride, Levosalbutamol Sulphate and Guaiphenesin Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ambroxol Hydrochloride	I.P.	15 mg
Levosalbutamol Sulphate (eq. to Levosalbutamol)	I.P.	0.50 mg
Guaiphenesin	I.P.	50 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Lycopene Enriched with Antioxidants, Multivitamin and Multimineral Syrup

Composition	Standard	Quantity (per 10 ml)
Each 10 ml contains :
Lycopene 10%	USP	2000 mcg
Niacinamide	I.P.	25 mg
Folic Acid	I.P.	100 mcg
Selenium Dioxide Monohydrate (eq. to Selenium)	B.P.	35 mcg
Zinc (as Zinc Gluconate USP)		3 mg
Iodine (as Potassium Iodide IP)		100 mcg
Copper (as Cupric Sulphate USP)		500 mcg
Vitamin B12	I.P.	1 mcg
Vitamin B6	I.P.	1.5 mg
Excipients		q.s.
In a flavoured base		q.s.
Appropriate overages of vitamins added to compensate for any loss on storage
Approved colour used

Aceclofenac and Paracetamol Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Aceclofenac	I.P.	50 mg
Paracetamol	I.P.	125 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Calcium Citrate Malate, Magnesium, Zinc,Vitamin D3, Methylcobalamin, L-Methylfolate Calcium & Pyridoxal-5 Phosphate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Calcium Citrate Malate (eq. to elemental Calcium)	I.P.	1250/250 mg
Magnesium Hydroxide (eq. to elemental Magnesium)	I.P.	75 mg
Zinc Sulphate Monohydrate (eq. to elemental Zinc)	I.P.	5 mg
Vitamin D3 (as stabilized)	I.P.	2000 IU
Methylcobalamin	I.P.	1500 mcg
L-Methylfolate Calcium	USP	1 mg
Pyridoxal-5 Phosphate		20 mg
Excipients		q.s.
Approved colour used

Vitamin D3 (Cholecalciferol) Drops

Composition	Standard	Quantity (per ml)
Each 1 ml contains :
Vitamin D3 (Cholecalciferol)	I.P.	800 IU
Excipients		q.s.
In a flavoured Palatable base		q.s.
Approved Colour used

Fungal Diastase and Pepsin syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Fungal Diastase (1:1200) (Derived from Aspergillus oryzae, digest not less than 60 gm of cooked starch)	I.P.	50 mg
Pepsin (1:3000) (Digest not less than 60 gm of coagulated egg albumin)	I.P.	10 mg
Excipients		q.s.
In a Flavoured Palatable base		q.s.
Approved Colour used
Dosage: Adult: One teaspoonful immediately after the meal. Children: Half the adult dose. As directed by the physician.

Clarithromycin Tablets I.P. 500 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Clarithromycin	I.P.	500 mg
Excipients		q.s.
Approved Colour used

Azithromycin Oral Suspension I.P.

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Azithromycin Dihydrate (eq. to anhydrous Azithromycin)	I.P.	200 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Cilnidipine Tablets I.P 10 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Cilnidipine	I.P.	10 mg
Excipients		q.s.
Approved Colour used

Ferrous Ascorbate And Folic Acid Suspension

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ferrous Ascorbate (eq. to elemental iron)		30 mg
Folic Acid	I.P.	550 mcg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

Linagliptin Tablets 5 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Linagliptin		5 mg
Excipients		q.s.
Approved Colour used

Terbutaline Sulphate, Bromhexine Hydrochloride, Guiaphenesin and Menthol Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml (one teaspoonful) contains :
Terbutaline Sulphate	I.P.	1.25 mg
Bromhexine Hydrochloride	I.P.	4 mg
Guaiphenesin	I.P.	50 mg
Menthol	I.P.	1 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Sitagliptin Phosphate Tablets I.P 100mg

Composition	Standard	Quantity
Each film coated tablet contains :
Sitagliptin Phosphate Monohydrate (Eq. to Sitagliptin)	I.P.	100 mg
Excipients		q.s.
Approved Colour used

Piracetam Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Piracetam	I.P.	500 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

Sitagliptin Phosphate Tablets I.P 50mg

Composition	Standard	Quantity
Each film coated tablet contains :
Sitagliptin Phosphate Monohydrate (Eq. to Sitagliptin)	I.P.	50 mg
Excipients		q.s.
Approved Colour used

Febuxostat Tablets 20 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Febuxostat		20 mg
Excipients		q.s.
Approved Colour used

Fenofibrate Tablets I.P 160 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Fenofibrate	I.P.	160 mg
Excipients		q.s.
Approved colour used

Montelukast Sodium and Levocetirizine Dihydrochloride Suspension (For Paediatric Use Only)

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Montelukast Sodium (eq. to Montelukast)	I.P.	4 mg
Levocetirizine Dihydrochloride	I.P.	2.5 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Colour: Approved colour used

Fenofibrate Tablets I.P 145mg

Composition	Standard	Quantity
Each film coated tablet contains :
Fenofibrate	I.P.	145 mg
Excipients		q.s.
Approved colour used

Etamsylate & Tranexamic Acid Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Etamsylate	B.P.	250 mg
Tranexamic Acid	I.P.	250 mg
Excipients		q.s.
Approved Colour used

Amlodipine Besylate and Metoprolol Succinate (ER)Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Amlodipine Besylate (Eq. to Amlodipine)	I.P.	5 mg
Metoprolol Succinate (eq. to Metoprolol Tartrate, Extended Released)	I.P.	23.75 mg/25 mg
Excipients		q.s.
Approved Colour used

Ferrous Ascorbate & Folic Acid Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Ferrous Ascorbate (eq. to elemental iron)	I.P.	100 mg
Folic Acid	I.P.	1.5 mg
Excipients		q.s.
Approved Colour used

Disulfiram Tablets I.P 500mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Disulfiram	I.P.	500 mg
Excipients		q.s.
Approved colour used

Disulfiram Tablets I.P 250mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Disulfiram	I.P.	250 mg
Excipients		q.s.
Approved colour used

Ursodeoxycholic Acid SR Tablets 300mg

Composition	Standard	Quantity
Each film coated sustained release tablet contains :
Ursodeoxycholic Acid	I.P.	300 mg
Excipients		q.s.
Approved colour used

Etoricoxib and Thiocolchicoside Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Etoricoxib	I.P.	60 mg
Thiocolchicoside	I.P.	8 mg
Excipients		q.s.

Piracetam Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Piracetam	I.P.	800 mg
Excipients		q.s.
Approved Colour used

Rifaximin Tablets 550mg

Composition	Standard	Quantity
Each film coated tablet contains :
Rifaximin	I.P.	550 mg
Excipients		q.s.
Approved colour used

Rifaximin Tablets 400mg

Composition	Standard	Quantity
Each film coated tablet contains :
Rifaximin	I.P.	400 mg
Excipients		q.s.
Approved colour used

Rifaximin Tablets 200mg

Composition	Standard	Quantity
Each film coated tablet contains :
Rifaximin	I.P.	200 mg
Excipients		q.s.
Approved colour used

Telmisartan and Amlodipine Besilate Tablets I.P

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Telmisartan	I.P.	40 mg
Amlodipine Besilate (eq. to Amlodipine)	I.P.	5 mg
Excipients		q.s.

Rifaximin Tabs 200mg

Each unc

Composition	Standard	Quantity
Each uncoated tablet contains :
Rifaximin		200 mg
Excipients		q.s.
Approved colour used

Rifaximin Tabs 400mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Rifaximin		400 mg
Excipients		q.s.
Approved colour used

Metronidazole & Furazolidone Bolus (only veterinary use)

Composition	Standard	Quantity
Each bolus contains :
Metronidazole	I.P.	1 g
Furazolidone	I.P.	200 mg
Excipients		q.s.
Approved colour used

Sulphadiazine & Trimethoprim Bolus I.P. (only veterinary use)

Composition	Standard	Quantity
Each bolus contains :
Sulphadiazine	I.P.	1000 mg
Trimethoprim	I.P.	200 mg
Excipients		q.s.
Approved colour used

Flunixin Meglumine & Serratiopeptidase Bolus (only veterinary use)

Composition	Standard	Quantity
Each uncoated bolus contains :
Flunixin Meglumine (eq. to Flunixin)	I.P.	1000 mg
Serratiopeptidase (eq. to enzyme activity 2,00,000 units, as enteric coated granules)	I.P.	100 mg
Excipients		q.s.
Approved Colour used

Oxfendazole Bolus (only veterinary use)

Composition	Standard	Quantity
Each uncoated bolus contains :
Oxfendazole	I.P.	2200 mg
Excipients		q.s.
Approved Colour used

Calcium Carbonate, Vitamin D3, Methylcobalamin, L-Methylfolate Calcium & Pyridoxal-5 Phosphate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Calcium Carbonate (Eq. to Elemental Calcium)	I.P.	500 mg
Vitamin D3	I.P.	2000 IU
Methylcobalamin	I.P.	1500 mcg
L-Methylfolate Calcium		1 mg
Pyridoxal-5 Phosphate		20 mg
Excipients		q.s.
Approved Colour used

Calcium, Vitamin D3, Methylcobalamin, L-Methylfolate Calcium & Pyridoxal-5 Phosphate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Calcium Carbonate (from an Organic source of Oyster Shell) Eq. to Elemental Calcium	I.P.	500 mg
Vitamin D3	I.P.	2000 IU
Methylcobalamin	I.P.	1500 mcg
L-Methylfolate Calcium		1 mg
Pyridoxal-5 Phosphate		0.5 mg
Excipients		q.s.
Approved Colour used

Clomipramine HCl Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Clomipramine Hydrochloride	I.P.	50 mg
Excipients		q.s.
Approved Colour used

100

Fluvoxamine Maleate Tablets I.P 100 mg.

Composition	Standard	Quantity
Each film coated tablet contains :
Fluvoxamine Maleate	I.P.	100 mg
Excipients		q.s.
Approved Colour used

101

Fluvoxamine Maleate Tablets I.P 50 mg.

Composition	Standard	Quantity
Each film coated tablet contains :
Fluvoxamine Maleate	I.P.	50 mg
Excipients		q.s.
Approved Colour used

102

Procyclidine HCl Tablets I.P 5mg.

Composition	Standard	Quantity
Each uncoated tablet contains :
Procyclidine Hydrochloride	I.P.	5 mg
Excipients		q.s.
Approved Colour used

103

Eperisone HCl Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Eperisone Hydrochloride		50 mg
Excipients		q.s.
Approved Colour used

104

Methylcobalamin, Alpha Lipoic Acid, Benfotiamine, Folic Acid, Chromium Polynicotinate, Inositol, Pyridoxine HCl, Vitamin D3 & Calcium Carbonate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Methylcobalamin	I.P.	1500 mcg
Alpha Lipoic Acid	I.P.	100 mg
Benfotiamine	USP	150 mg
Folic Acid	I.P.	1.5 mg
Chromium Polynicotinate		200 mcg
Inositol	I.P.	100 mg
Pyridoxine Hydrochloride	I.P.	3 mg
Vitamin D3	I.P.	1000 IU
Calcium Carbonate	I.P.	500 mg
Excipients		q.s.
Approved Colour used

105

Dapagliflozin and Metformin HCl (ER) Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Dapagliflozin Propanediol Monohydrate (Eq. to Dapagliflozin)		10 mg
Metformin HCl (as extended release form)	I.P.	500 mg
Excipients		q.s.
Approved Colour used

106

Vildagliptin Tablets I.P 50 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Vildagliptin	I.P.	50 mg
Excipients		q.s.
Approved Colour used

107

Rosuvastatin and Fenofibrate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Rosuvastatin Calcium (eq. to Rosuvastatin)	I.P.	10 mg
Fenofibrate	I.P.	145 mg
Excipients		q.s.
Approved Colour used

108

Bilastine and Montelukast Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Bilastine	I.P.	20 mg
Montelukast Sodium (Eq. to Montelukast)		10 mg
Excipients		q.s.
Approved Colour used

109

Duloxetine Gastro-resistant Tablets I.P. 30mg

Composition	Standard	Quantity
Each enteric coated tablet contains :
Duloxetine Hydrochloride (eq. to Duloxetine)	I.P.	30 mg
Excipients		q.s.
Approved Colour used

110

Duloxetine Gastro-resistant Tablets I.P. 20mg

Composition	Standard	Quantity
Each enteric coated tablet contains :
Duloxetine Hydrochloride (eq. to Duloxetine)	I.P.	20 mg
Excipients		q.s.
Approved Colour used

111

Naproxen Tablets I.P 500mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Naproxen	I.P.	500 mg
Excipients		q.s.
Approved Colour used

112

Propranolol Hydrochloride Tablets I.P 40mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Propranolol Hydrochloride	I.P.	40 mg
Excipients		q.s.
Approved Colour used

113

Tadalafil Tablets I.P 10mg

Composition	Standard	Quantity
Each film coated tablet contains :
Tadalafil	I.P.	10 mg
Excipients		q.s.
Approved Colour used

114

Drotaverine Hydrochloride Tablets I.P 40mg

Composition	Standard	Quantity
Each film coated tablet contains :
Drotaverine Hydrochloride	I.P.	40 mg
Excipients		q.s.
Approved Colour used

115

Gabapentin Tablets I.P 300 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Gabapentin	I.P.	300 mg
Excipients		q.s.
Approved Colour used

116

Gabapentin Tablets I.P 100 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Gabapentin	I.P.	100 mg
Excipients		q.s.
Approved Colour used

117

Rosuvastatin Calcium and Ezetimibe Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Rosuvastatin Calcium (eq. to Rosuvastatin)	I.P.	40 mg
Ezetimibe	I.P.	10 mg
Excipients		q.s.
Approved Colour used

118

Rosuvastatin Calcium and Ezetimibe Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Rosuvastatin Calcium (eq. to Rosuvastatin)	I.P.	20 mg
Ezetimibe	I.P.	10 mg
Excipients		q.s.
Approved Colour used

119

Amlodipine Besylate and Metoprolol Succinate (ER) Tablets

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Amlodipine Besylate (Eq. to Amlodipine)	I.P.	5 mg
Metoprolol Succinate (Eq. to Metoprolol Tartrate, extended release)	I.P.	47.50 mg / 50 mg
Excipients		q.s.
Approved Colour used

120

Voglibose and Metformin Hydrochloride (SR) Tablets

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Voglibose	I.P.	0.3 mg
Metformin Hydrochloride (sustained released)	I.P.	500 mg
Excipients		q.s.
Approved Colour used

121

Amitriptyline Hydrochloride Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Amitriptyline Hydrochloride	I.P.	50 mg
Excipients	q.s.
Approved Colour used

122

Amitriptyline Hydrochloride Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Amitriptyline Hydrochloride	I.P.	25 mg
Excipients		q.s.
Approved Colour used

123

Amitriptyline Hydrochloride Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Amitriptyline Hydrochloride	I.P.	10 mg
Excipients		q.s.
Approved Colour used

124

Flavoxate Hydrochloride Tablets I.P 200mg

Composition	Standard	Quantity
Each film coated tablet contains :
Flavoxate Hydrochloride	I.P.	200 mg
Excipients		q.s.
Approved Colour used

125

Telmisartan 40 mg & Cilnidipine 10 mg Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Telmisartan	I.P.	40 mg
Cilnidipine	I.P.	10 mg
Excipients		q.s.
Approved Colour used

126

Ginkgo biloba Dry Extract Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Ginkgo biloba dry extract (containing 9.6 mg of ginkgo flavone glycosides)	I.P.	40 mg
Excipients		q.s.
Approved colour used

127

L-Carnitine L-Tartrate, Methylcobalamin & Folic Acid Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
L-Carnitine L-Tartrate Eq. to L-Carnitine		500 mg
Methylcobalamin	I.P.	1500 mcg
Folic Acid		1.5 mg
Excipients		q.s.
Approved colour used

128

Methylcobalamin, L-Methyl Folate & Pyridoxal-5 Phosphate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Methylcobalamin	I.P.	1500 mcg
L-5 Methyltetrahydrofolate Calcium (eq. to L-Methyl Folate)		1 mg
Pyridoxal-5 Phosphate		0.5 mg
Excipients		q.s.
Approved colour used

129

Esomeprazole Gastro-resistant Tablets I.P 40mg

Composition	Standard	Quantity
Each enteric coated tablet contains :
Esomeprazole Magnesium Trihydrate (eq. to Esomeprazole)	I.P.	40 mg
Excipients		q.s.
Approved colour used

130

Esomeprazole Gastro-resistant Tablets I.P 20mg

Composition	Standard	Quantity
Each enteric coated tablet contains :
Esomeprazole Magnesium Trihydrate (eq. to Esomeprazole)	I.P.	20 mg
Excipients		q.s.
Approved colour used

131

Citicoline and Piracetam Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Citicoline Sodium (eq. to Citicoline)	I.P.	500 mg
Piracetam	I.P.	800 mg
Excipients		q.s.
Approved Colour used

132

Ambroxol Hydrochloride, Levocetirizine Hydrochloride, Guaiphenesin and Menthol Syrup

Composition	Standard	Quantity
Each 5 ml contains:
Ambroxol Hydrochloride	I.P.	15 mg
Levocetirizine Hydrochloride	I.P.	2.5 mg
Guaiphenesin	I.P.	50 mg
Menthol	I.P.	1 mg
In a flavoured syrup base		q.s.
Excipients		q.s.
Colour		Approved colour used

133

Magaldrate and Simethicone Oral Suspension U.S.P.

Composition	Standard	Quantity
Each 5 ml contains:
Magaldrate (anhydrous)	I.P.	400 mg
Simethicone	I.P.	20 mg
Sorbitol Solution 70% (Non-crystallizing)	I.P.	q.s.
Purified Water	I.P.	q.s.
Excipients		q.s.
Approved Colour used
Dosage: Adults & Children over 12 years: 1–2 teaspoonfuls between meals & at bedtime. Children 5–12 years: Half of the above dose or as directed by the physician.

134

Dextromethorphan Hydrobromide, Chlorpheniramine Maleate and Phenylepherine Hydrochloride Syrup

Composition	Standard	Quantity
Each 5 ml (one teaspoonful) contains :
Dextromethorphan Hydrobromide	I.P.	10 mg
Chlorpheniramine Maleate	I.P.	2 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used
Dosage: Adults: 10 ml, 3–4 times a day Children (2–6 years): 2.5 ml, 3–4 times a day Children (6–12 years): 5 ml, 3–4 times a day

135

Rosuvastatin Calcium Tablets I.P. 40 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Rosuvastatin Calcium (eq. to Rosuvastatin)	I.P.	40 mg
Excipients		q.s.
Approved Colour used

136

Cyproheptadine Hydrochloride and Tricholine Citrate Syrup

Composition	Standard	Quantity
Each 5 ml contains :
Cyproheptadine Hydrochloride (anhydrous)	I.P.	2 mg
Tricholine Citrate (65%)		275 mg
Sorbitol Solution 70% (Non-crystallizing)	I.P.	q.s.
Excipients		q.s.
In a Flavoured Syrup base		q.s.
Approved Colour used

137

Terbutaline Sulphate, Ambroxol Hydrochloride, Guaiphenesin and Menthol Syrup

Composition	Standard	Quantity
Each 5 ml contains :
Terbutaline Sulphate	I.P.	2.5 mg
Ambroxol Hydrochloride	I.P.	30 mg
Guaiphenesin	I.P.	100 mg
Menthol	I.P.	2.5 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

138

Deflazacort Oral Suspension

Composition	Standard	Quantity
Each 5 ml contains :
Deflazacort		6 mg
In a flavoured syrup base		q.s.
Excipients		q.s.
Approved Colour used

139

Ambroxol Hydrochloride, Levosalbutamol Sulphate and Guaiphenesin Syrup

Composition	Standard	Quantity
Each 5 ml contains :
Ambroxol Hydrochloride	I.P.	30 mg
Levosalbutamol Sulphate eq. to Levosalbutamol	I.P.	1 mg
Guaiphenesin	I.P.	50 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved colour used

140

Paracetamol, Phenylephrine HCl, Chlorpheniramine Maleate, Sodium Citrate and Menthol syrup Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Paracetamol	I.P.	125 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Chlorpheniramine Maleate	I.P.	0.5 mg
Sodium Citrate	I.P.	60 mg
Menthol	I.P.	1 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

141

Metformin Hydrochloride Sustained Released Tablets I.P.

Composition	Standard	Quantity
Each uncoated sustained release tablet contains :
Metformin Hydrochloride	I.P.	1000 mg
Excipients		q.s.
Approved Colour used

142

Ambroxol Hydrochloride, Terbutaline Sulphate, Guaiphenesin and Menthol Syrup

Composition	Standard	Quantity (per 5 ml)
Each 5 ml contains :
Ambroxol Hydrochloride	I.P.	15 mg
Terbutaline Sulphate	I.P.	1.25 mg
Guaiphenesin	I.P.	50 mg
Menthol	I.P.	2.5 mg
Excipients		q.s.
In a flavoured syrup base		q.s.
Approved Colour used

143

Dextromethorphan Hydrobromide, Chlorpheniramine Maleate and Phenylepherine Hydrochloride Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Dextromethorphan Hydrobromide	I.P.	10 mg
Chlorpheniramine Maleate	I.P.	2 mg
Phenylepherine Hydrochloride	I.P.	5 mg
Excipients		q.s.
Colour: Ponceau-4R

144

Lansoprazole Orally Disintegrating Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Lansoprazole (as enteric coated pellets)	I.P.	15 mg
Excipients		q.s.
Approved Colour used

145

Aceclofenac and Paracetamol Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Aceclofenac	I.P.	100 mg
Paracetamol	I.P.	325 mg
Excipients		q.s.
Approved Colour used

146

Fexofenadine and Montelukast Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Fexofenadine Hydrochloride	I.P.	120 mg
Montelukast Sodium (eq. to Montelukast)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

147

Telmisartan 40 mg and Chlorthalidone 12.5 mg Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Telmisartan	I.P.	40 mg
Chlorthalidone	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

148

Silodosin 8mg & Dutasteride 0.5mg Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Silodosin		8 mg
Dutasteride (as uncoated tablet)	I.P.	0.5 mg
Excipients		q.s.
Approved colour used in empty capsule shells

149

Diacerein Capsules 50mg I.P

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Diacerein	I.P.	50 mg
Excipients		q.s.
Approved colour used in empty capsule shells

150

Telmisartan 80 mg and Chlorthalidone 12.5 mg Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Telmisartan	I.P.	80 mg
Chlorthalidone	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

151

Calcium Dobesilate Capsules 500 mg.

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Calcium Dobesilate Monohydrate	I.P.	500 mg
Excipients		q.s.
Approved colour used in empty capsule shells

152

Metoprolol Succinate (ER) Tablets I.P.

Composition	Standard	Quantity
Each uncoated extended release tablet contains :
Metoprolol Succinate (eq. to Metoprolol Tartrate, extended release)	I.P.	50 mg
(Metoprolol Succinate actual strength)	I.P.	47.50 mg
Excipients		q.s.
Approved Colour used

153

Alpha Lipoic Acid, Methylcobalamin, Pyridoxine Hydrochloride, Folic Acid, Benfotiamine, Chromium Picolinate & Biotin Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Alpha Lipoic Acid	USP	100 mg
Methylcobalamin	I.P.	1500 mcg
Pyridoxine Hydrochloride	I.P.	3 mg
Folic Acid	I.P.	1.5 mg
Benfotiamine	I.P.	50 mg
Chromium Picolinate eq. to Chromium	USP	200 mcg
Biotin	USP	5 mg
Excipients		q.s.
Approved colour used in empty capsule shells

154

Itraconazole Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Itraconazole (as pellets)	I.P.	100 mg
Excipients		q.s.
Approved colour used in empty capsule shells & pellets

155

Aspirin Gasto-resistant & Rosuvastatin Capsules I.P

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Aspirin (as enteric coated pellets)	I.P.	75 mg
Rosuvastatin Calcium eq. to Rosuvastatin (as pellets)	I.P.	20 mg
Excipients		q.s.
Approved Colour used in empty capsule shells & pellets

156

Metoprolol Succinate (ER) Tablets I.P.

Composition	Standard	Quantity
Each uncoated extended release tablet contains :
Metoprolol Succinate (eq. to Metoprolol Tartrate, extended release)	I.P.	25 mg
Excipients		q.s.
Approved Colour used

157

Diclofenac Potassium Paracetamol and Serratiopeptidase Tablets (Warning: Overdose of this drug has potential of severe liver injury & allergic reactions (e.g. swelling of face, mouth & throat, difficulty in breathing, itching or rashes)

Composition	Standard	Quantity
Each film coated tablet contains :
Diclofenac Potassium	B.P.	50 mg
Paracetamol	I.P.	325 mg
Serratiopeptidase (as enteric coated granules, eq. to enzymatic activity 20,000 units)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

158

Glimepiride, Metformin HCl (SR) and Pioglitazone Tablets [Note: Package Insert as per H&FW Deptt. Notification No. GSR520(E) dated 31.07.2013 to to be enclosed]

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Glimepiride	I.P.	1 mg
Metformin Hydrochloride (In sustained release form)	I.P.	500 mg
Pioglitazone Hydrochloride eq. to Pioglitazone	I.P.	15 mg
Excipients		q.s.
Approved Colour used

159

Itraconazole Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Itraconazole (as pellets)	I.P.	200 mg
Excipients		q.s.
Approved Colour used in empty capsule shells

160

Mefenamic Acid Capsules I.P 250 mg

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Mefenamic Acid	I.P.	250 mg
Excipients		q.s.
Approved colour used in empty capsule shells

161

Glimepiride, Metformin HCl (SR) and Pioglitazone Tablets [Note: Package Insert as per H&FW Deptt. Notification No. GSR520(E) dated 31.07.2013 to to be enclosed]

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Glimepiride	I.P.	2 mg
Metformin Hydrochloride (In sustained release form)	I.P.	500 mg
Pioglitazone Hydrochloride eq. to Pioglitazone	I.P.	15 mg
Excipients		q.s.
Approved Colour used

162

Diclofenac Potassium and Serratiopeptidase Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Diclofenac Potassium	B.P.	50 mg
Serratiopeptidase (as enteric coated granules eq. to enzymatic activity 20,000 units)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

163

Thiocolchicoside Capsules I.P 8 mg

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Thiocolchicoside	I.P.	8 mg
Excipients		q.s.
Approved colour used in empty capsule shells

164

Thiocolchicoside Capsules I.P 4 mg

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Thiocolchicoside	I.P.	4 mg
Excipients		q.s.
Approved colour used in empty capsule shells

165

Rabeprazole and Ondansetron Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Rabeprazole Sodium	I.P.	20 mg
Ondansetron Hydrochloride (eq. to Ondansetron)	I.P.	4 mg
Excipients		q.s.
Approved Colour used

166

Doxylamine Succinate, Pyridoxine HCl & Folic Acid Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Doxylamine Succinate	USP	10 mg
Pyridoxine Hydrochloride	I.P.	10 mg
Folic Acid	I.P.	2.5 mg
Excipients		q.s.
Approved Colour used

167

Clindamycin Hydrochloride Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Clindamycin Hydrochloride eq. to Clindamycin	I.P.	300 mg
Excipients		q.s.
Approved colour used in empty capsule shells

168

Aceclofenac, Paracetamol, Cetirizine Dihydrochloride, Phenylephrine HCl and CaffeineTablets

Composition

Standard

Quantity

Each uncoated tablet contains :

Aceclofenac

I.P.

100 mg

Paracetamol

I.P.

325 mg

Cetirizine Dihydrochloride

I.P.

10 mg

Phenylephrine Hydrochloride

I.P.

5 mg

Caffeine

I.P.

25 mg

Excipients

q.s.

Approved Colour used

169

Rosuvastatin and Aspirin Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rosuvastatin Calcium eq. to Rosuvastatin (as pellets)	I.P.	10 mg
Aspirin (as enteric coated pellets)	I.P.	75 mg
Excipients		q.s.
Approved colour used

170

Ferrous Ascorbate, Folic acid and Zinc Sulphate Monohydrate Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Ferrous Ascorbate	I.P.	100 mg
Folic Acid	I.P.	1.5 mg
Zinc Sulphate Monohydrate (eq. to Elemental Zinc)	I.P.	22.5 mg
Excipients	q.s.
Approved Colour used

171

Rosuvastatin and Aspirin Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rosuvastatin Calcium eq. to Rosuvastatin (as granules)	I.P.	20 mg
Aspirin (as enteric coated tablets)	I.P.	75 mg
Excipients		q.s.
Approved colour used

172

Rosuvastatin and Aspirin Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rosuvastatin Calcium eq. to Rosuvastatin (as granules)	I.P.	10 mg
Aspirin (as enteric coated tablets)	I.P.	75 mg
Excipients		q.s.
Approved colour used

173

Acebrophylline Sustained Release, Fexofenadine HCl and Montelukast Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Acebrophylline (as sustained release form)		200 mg
Fexofenadine Hydrochloride	I.P.	120 mg
Montelukast Sodium (eq. to Montelukast)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

174

Levocetirizine Dihydrochloride, Montelukast and Ambroxol HCl (SR) Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Levocetirizine Dihydrochloride	I.P.	5 mg
Montelukast Sodium (eq. to Montelukast)	I.P.	10 mg
Ambroxol Hydrochloride (as sustained release)	I.P.	75 mg
Excipients		q.s.
Approved Colour used

175

Naproxen and Domperidone Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Naproxen	I.P.	500 mg
Domperidone	I.P.	10 mg
Excipients		q.s.
Approved Colour used

176

Doxycycline & Lactic Acid Bacillus Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Doxycycline Hydrochloride eq. to Doxycycline	I.P.	100 mg
Lactic Acid Bacillus		60 Million Spores
Excipients		q.s.
Approved colour used in capsule shells

177

Rosuvastatin, Clopidogrel and Aspirin Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rosuvastatin Calcium eq. to Rosuvastatin (as pellets)	I.P.	10 mg
Clopidogrel Bisulphate eq. to Clopidogrel (as pellets)	I.P.	75 mg
Aspirin (as enteric coated pellets)	I.P.	75 mg
Excipients		q.s.
Approved colour used

178

Rabeprazole Sodium(EC) and Aceclofenac (SR) Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rabeprazole Sodium (as enteric coated pellets)	I.P.	20 mg
Aceclofenac (as sustained release pellets)	I.P.	200 mg
Excipients		q.s.
Approved colour used in empty capsule shells

179

Esomeprazole (EC) and Itopride HCl (SR) Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Esomeprazole Magnesium Trihydrate eq. to Esomeprazole (as enteric coated pellets)	I.P.	40 mg
Itopride Hydrochloride (as sustained released pellets)	I.P.	150 mg
Excipients		q.s.
Approved colour used in empty capsule shells

180

Omeprazole Gastro-resistant Capsules I.P.

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Omeprazole (as gastro resistant pellets)	I.P.	20 mg
Excipients		q.s.
Approved colour used in capsule shells

181

Teneligliptin and Metformin Hydrochloride (ER)Tablets

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Teneligliptin Hydrobromide Hydrate (eq. to Teneligliptin)	I.P.	20 mg
Metformin Hydrochloride (as extended release)	I.P.	500 mg
Excipients	q.s.
Approved Colour used

182

Methylcobalamin, Alpha Lipoic Acid, Benfotiamine, Pyridoxine HCl, Inositol and Folic Acid Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Methylcobalamin	I.P.	1000 mcg
Alpha Lipoic Acid	I.P.	200 mg
Benfotiamine		100 mg
Folic Acid	I.P.	1.5 mg
Pyridoxine HCl	I.P.	3 mg
Inositol	USP	100 mg
Excipients		q.s.
Approved colour used in empty capsule shells

183

Methylcobalamin, Alpha Lipoic Acid, Benfotiamine, Pyridoxine HCl, Inositol and Folic Acid Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Methylcobalamin	I.P.	1000 mcg
Alpha Lipoic Acid	I.P.	200 mg
Benfotiamine		100 mg
Folic Acid	I.P.	1.5 mg
Pyridoxine HCl	I.P.	3 mg
Inositol	USP	100 mg
Excipients		q.s.
Approved colour used in empty capsule shells

184

Methylcobalamin, Alpha Lipoic Acid, Thiamine Mononitrate, Pyridoxine Hydrochloride, and Folic Acid Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Methylcobalamin	I.P.	1500 mcg
Alpha Lipoic Acid	I.P.	100 mg
Thiamine Mononitrate	I.P.	10 mg
Pyridoxine Hydrochloride	I.P.	3 mg
Folic Acid	I.P.	1.5 mg
Excipients		q.s.
Appropriate overages of vitamins are added to compensate loss on storage
Approved colour used in empty capsule shells

185

Paracetamol, Phenylephrine HCl and Cetirizine HCl Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Paracetamol	I.P.	325 mg
Phenylephrine Hydrochloride	I.P.	5 mg
Cetirizine Hydrochloride	I.P.	5 mg
Excipients		q.s.
Approved Colour used

186

Pregabalin and Methylcobalamin Capsules I.P

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Pregabalin	I.P.	75 mg
Methylcobalamin	I.P.	750 mcg
Excipients		q.s.
Approved colour used in empty capsule shells
Appropriate overages of vitamin added to compensate loss on storage

187

Flupentixol and Melitracen Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Flupentixol Hydrochloride (Eq. to Flupentixol)	B.P.	0.5 mg
Melitracen Hydrochloride (Eq. to Melitracen)		10 mg
Excipients		q.s.
Approved Colour used

188

Esomeprazole and Levosulpride Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Esomeprazole Magnesium Trihydrate eq. to Esomeprazole (as enteric coated pellets)	I.P.	40 mg
Levosulpiride (as sustained released pellets)		75 mg
Excipients		q.s.
Approved colour used in empty capsule shells

189

Sitagliptin Phosphate and Metformin Hydrochloride Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Sitagliptin Phosphate Monohydrate (Eq. to Sitagliptin)	I.P.	50 mg
Metformin Hydrochloride	I.P.	500 mg
Excipients		q.s.
Approved Colour used

190

Pantoprazole and Levosulpiride Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Pantoprazole Sodium eq. to Pantoprazole (as enteric coated pellets)	I.P.	40
Levosulpiride (as sustained released pellets)		75
Excipients
Approved colour used in empty capsule shells

191

Fexofenadine and Montelukast Chewable Tablets

Composition	Standard	Quantity
Each uncoated chewable tablet contains :
Fexofenadine Hydrochloride	I.P.	120 mg
Montelukast Sodium (eq. to Montelukast)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

192

Levetiracetam Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Levetiracetam	I.P.	500 mg
Excipients		q.s.
Approved Colour used

193

Rebeprazole and Itopride Hydrochloride Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rabeprazole Sodium (as enteric coated pellets)	I.P.	20 mg
Itopride Hydrochloride (as sustained released pellets)		150 mg
Excipients		q.s.
Approved colour used in empty capsule shells

194

Esomeprazole and Domperidone Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Esomeprazole Magnesium Trihydrate eq. to Esomeprazole (as enteric coated pellets)	I.P.	40 mg
Domperidone (as sustained released pellets)	I.P.	30 mg
Excipients		q.s.
Approved colour used in empty capsule shells

195

Tamsulosin HCl (MR) and Dutasteride Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Tamsulosin Hydrochloride (as modified release)	I.P.	0.4 mg
Dutasteride	I.P.	0.5 mg
Excipients		q.s.
Approved Colour used

196

Rabeprazole and Levosulpride Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rabeprazole Sodium (as enteric coated pellets)	I.P.	20 mg
Levosulpiride (as sustained released pellets)		75 mg
Excipients		q.s.
Approved colour used in empty capsule shells

197

Pantoprazole Gasto-resistant and Domperidone Prolonged-release Capsules I.P

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Pantoprazole Sodium eq. to Pantoprazole (as gastro-resistant pellets)	I.P.	40 mg
Domperidone (as prolonged-release pellets)	I.P.	30 mg
Excipients		q.s.
Approved colour used in empty capsule shells

198

Rabeprazole and Domperidone Capsule

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Rabeprazole Sodium (as enteric coated pellets)	I.P.	20 mg
Domperidone (as sustained released pellets)	I.P.	30 mg
Excipients		q.s.
Approved colour used in empty capsule shells

199

Omeprazole and Domperidone Capsules I.P

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Omeprazole (as enteric coated pellets)	I.P.	20 mg
Domperidone	I.P.	10 mg
Excipients		q.s.
Approved colour used in empty capsule shells

200

Methylcobalamin, Alpha Lipoic Acid, Inositol, Folic Acid, Chromium Polynicotinate, Selenium Dioxide and Benfotiamine Capsules

Composition	Standard	Quantity
Each hard gelatin capsule contains :
Methylcobalamin	I.P.	1500 mcg
Alpha Lipoic Acid	USP	100 mg
Inositol	USP	100 mg
Folic Acid	I.P.	1.5 mg
Chromium Polynicotinate	USP	200 mcg
Selenium Dioxide	B.P.	55 mcg
Benfotiamine	USP	150 mg
Excipients		q.s.
Approved colour used in empty capsule shells

201

Vildagliptin and Metformin Hydrochloride Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Vildagliptin	I.P.	50 mg
Metformin Hydrochloride	I.P.	1000 mg
Excipients		q.s.
Approved Colour used

202

Vildagliptin and Metformin Hydrochloride Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Vildagliptin	I.P.	50 mg
Metformin Hydrochloride	I.P.	850 mg
Excipients		q.s.
Approved Colour used

203

Vildagliptin and Metformin Hydrochloride Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Vildagliptin	I.P.	50 mg
Metformin Hydrochloride	I.P.	500 mg
Excipients	q.s.
Approved Colour used

204

Metformin HCl Prolonged release and Glimepiride Tablets I.P

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Metformin Hydrochloride (In Prolonged release form)	I.P.	500 mg
Glimepiride	I.P.	2 mg
Excipients	q.s.
Approved Colour used

205

Metformin HCl Prolonged release and Glimepiride Tablets I.P

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Metformin Hydrochloride (In Prolonged release form)	I.P.	500 mg
Glimepiride	I.P.	1 mg
Excipients		q.s.
Approved Colour used

206

Citicoline and Piracetam Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Citicoline Sodium (eq. to Citicoline)	I.P.	500 mg
Piracetam	I.P.	400 mg
Excipients		q.s.
Approved Colour used

207

Drotaverine Hydrochloride and Mefenamic Acid Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Drotaverine Hydrochloride	I.P.	80 mg
Mefenamic Acid	I.P.	250 mg
Excipients		q.s.
Approved Colour used

208

Trypsin,Bromelain, Rustoside Trihydrate and Aceclofenac Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Trypsin	B.P.	48 mg
Bromelain		90 mg
Rustoside Trihydrate	B.P.	100 mg
Aceclofenac	I.P.	100 mg
Excipients		q.s.
Approved Colour used

209

Glimepiride and Metformin Hydrochloride (SR) Tablets

Composition	Standard	Quantity
Each uncoated bilayered tablet contains :
Glimepiride	I.P.	2 mg
Metformin Hydrochloride (sustained released)	I.P.	1000 mg
Excipients		q.s.
Approved Colour used

210

Diclofenac Potassium Paracetamol and Chlorzoxazone Tablets (Warning: Overdose of this drug has potential of severe liver injury & allergic reactions (e.g. swelling of face, mouth & throat, difficulty in breathing, itching or rashes)

Composition	Standard	Quantity
Each film coated tablet contains :
Diclofenac Potassium	B.P.	50 mg
Paracetamol	I.P.	325 mg
Chlorzoxazone	USP	250 mg
Excipients		q.s.
Approved Colour used

211

Gabapentin & Nortriptyline HCl Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Gabapentin	I.P.	400 mg
Nortriptyline Hydrochloride (Eq. to Nortriptyline)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

212

Ketorolac Tromethamine Dispersible Tablets 10mg

Composition	Standard	Quantity
Each uncoated dispersible tablet contains :
Ketorolac Tromethamine	I.P.	10 mg
Excipients		q.s.
Approved Colour used

213

Rabeprazole and Domperidone Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Rabeprazole Sodium	I.P.	20 mg
Domperidone	I.P.	10 mg
Excipients		q.s.
Approved Colour used

214

Amisulpiride Tablets IP 50 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Amisulpride	I.P.	50 mg
Excipients		q.s.
Approved colour used

215

Sildenafil Citrate Tablets I.P. 50 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Sildenafil Citrate (eq. to Sildenafil)	I.P.	50 mg
Excipients		q.s.
Approved Colour used

216

Tolperisone HCl and Diclofenac Sodium Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Tolperisone Hydrochloride		150 mg
Diclofenac Sodium	I.P.	50 mg
Excipients		q.s.
Approved Colour used

217

Cinnarizine and Domperidone Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Cinnarizine	I.P.	20 mg
Domperidone	I.P.	15 mg
Excipients		q.s.
Approved Colour used

218

Eperisone Hydrochloride and Paracetamol Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Eperisone Hydrochloride		50 mg
Paracetamol	I.P.	325 mg
Excipients		q.s.
Approved Colour used

219

Levosulpride Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Levosulpiride		50 mg
Excipients		q.s.
Approved Colour used

220

Terbinafine Tablets I.P 250 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Terbinafine Hydrochloride (eq. to Terbinafine)	I.P.	250 mg
Excipients		q.s.
Approved Colour used

221

Trypsin,Bromelain, Rustoside Trihydrate and Diclofenac Sodium Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Trypsin	B.P.	48 mg
Bromelain		90 mg
Rutoside Trihydrate	B.P.	100 mg
Diclofenac Sodium	I.P.	50 mg
Excipients		q.s.
Approved Colour used

222

Trypsin,Bromelain and Rustoside Trihydrate Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Trypsin	B.P.	48 mg
Bromelain		90 mg
Rutoside Trihydrate	B.P.	100 mg
Excipients		q.s.
Approved Colour used

223

Aceclofenac and Thiocolchicoside Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Aceclofenac	I.P.	100 mg
Thiocolchicoside	I.P.	8 mg
Excipients		q.s.
Approved Colour used

224

Levocetirizine Hydrochloride and Ambroxol Hydrochloride (SR) Tablets

Composition	Standard	Quantity
Each uncoated sustained released tablet contains :
Levocetirizine Hydrochloride	I.P.	5 mg
Ambroxol Hydrochloride (as sustained released)	I.P.	75 mg
Excipients		q.s.
Approved Colour used

225

Tranexamic Acid and Mefenamic Acid Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Tranexamic Acid	I.P.	500 mg
Mefenamic Acid	I.P.	250 mg
Excipients		q.s.
Approved Colour used

226

Etoricoxib and Paracetamol Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Etoricoxib	I.P.	60 mg
Paracetamol	I.P.	325 mg
Excipients		q.s.
Approved Colour used

227

Diclofenac Sodium and Serratiopeptidase Tablets

Composition	Standard	Quantity
Each enteric coated tablet contains :
Diclofenac Sodium	B.P.	50 mg
Serratiopeptidase (as enteric coated granules, eq. to enzymatic activity 20,000 units)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

228

Glucosamine, Methylsulphonylmethane and Diacerein Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Glucosamine Sulphate Potassium Chloride (eq. to Glucosamine)	USP	446 mg (750 mg eq.)
Methylsulphonylmethane	USP	250 mg
Diacerein	I.P.	50 mg
Excipients		q.s.
Approved Colour used

229

Montelukast and Levocetirizine Hydrochloride Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Levocetirizine Hydrochloride	I.P.	2.5 mg
Montelukast Sodium (eq. to Montelukast)	I.P.	4 mg
Excipients		q.s.
Approved Colour used

230

Aceclofenac Sustained Released Tablets 200mg

Composition	Standard	Quantity
Each uncoated sustained released tablet contains :
Aceclofenac	I.P.	200 mg
Excipients		q.s.
Approved Colour used

231

Lornoxicam and Paracetamol Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Lornoxicam		8 mg
Paracetamol	I.P.	325 mg
Excipients		q.s.
Approved Colour used

232

Lornoxicam and Paracetamol Tablets

Composition	Standard	Quantity
Each film coated tablet contains :
Lornoxicam		4 mg
Paracetamol	I.P.	325 mg
Excipients		q.s.
Approved Colour used

233

Metoprolol Succinate (ER) Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Metoprolol Succinate (eq. to Metoprolol Tartrate, extended released)	I.P.	47.50 mg (50 mg eq.)
Excipients		q.s.
Approved Colour used

234

Metoprolol Succinate (ER) Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Metoprolol Succinate (eq. to Metoprolol Tartrate, extended released)	I.P.	23.75 mg (25 mg eq.)
Excipients		q.s.
Approved Colour used

235

Mefenamic Acid and Dicyclomine HCl Tablets I.P

Composition	Standard	Quantity
Each uncoated tablet contains :
Mefenamic Acid	I.P.	250 mg
Dicyclomine Hydrochloride	I.P.	10 mg
Excipients		q.s.
Approved Colour used

236

Diclofenac Sodium and Paracetamol Tablets I.P (Warning: Overdose of this drug has potential of severe liver injury & allergic reactions (e.g. swelling of face, mouth & throat, difficulty in breathing, itching or rashes)

Composition

Standard

Quantity

Each uncoated tablet contains :

Diclofenac Sodium

I.P.

50 mg

Paracetamol

I.P.

325 mg

Excipients

q.s.

237

Amlodipine Besylate and Metoprolol Succinate (ER)Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Amlodipine Besylate (Eq. to Amlodipine)	I.P.	5 mg
Metoprolol Succinate (eq. to Metoprolol Tartrate, Extended Released)	I.P.	47.5 mg (50 mg eq.)
Excipients		q.s.
Approved Colour used

238

Amlodipine Besilate and Atenolol Tablets I.P.

Composition	Standard	Quantity
Each uncoated tablet contains :
Amlodipine Besilate (eq. to Amlodipine)	I.P.	5 mg
Atenolol	I.P.	50 mg
Excipients		q.s.
Approved Colour used

239

Amlodipine Besilate Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Amlodipine Besilate (eq. to Amlodipine)	I.P.	5 mg
Excipients		q.s.
Approved Colour used

240

Metformin Hydrochloride Sustained Released Tablets I.P.

Composition	Standard	Quantity
Each uncoated tablet contains :
Metformin Hydrochloride (sustained released)	I.P.	500 mg
Excipients		q.s.
Approved Colour used

241

Losartan Potassium and Hydrochlorothiazide Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Losartan Potassium	I.P.	50 mg
Hydrochlorothiazide	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

242

Losartan Potassium and Amlodipine Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Losartan Potassium	I.P.	50 mg
Excipients		q.s.
Approved Colour used

243

Losartan Potassium Tablets I.P. 50 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Losartan Potassium	I.P.	50 mg
Excipients		q.s.
Approved Colour used

244

Linezolid Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Linezolid	I.P.	600 mg
Excipients		q.s.
Approved Colour used

245

Olmesartan Medoxomil and Amlodipine Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Olmesartan Medoxomil	I.P.	40 mg
Amlodipine Besylate (eq. to Amlodipine)	I.P.	5 mg
Excipients		q.s.
Approved Colour used

246

Olmesartan Medoxomil 20 mg and Hydrochlorothiazide 12.5 mg Tablets I.P

Composition	Standard	Quantity
Each uncoated tablet contains :
Olmesartan Medoxomil	I.P.	20 mg
Hydrochlorothiazide	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

247

Olmesartan Medoxomil Tablets I.P. 40 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Olmesartan Medoxomil	I.P.	40 mg
Excipients		q.s.
Approved Colour used

248

Olmesartan Medoxomil Tablets I.P. 20 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Olmesartan Medoxomil	I.P.	20 mg
Excipients		q.s.
Approved Colour used

249

Loratadine Tablets I.P.

Composition	Standard	Quantity
Each uncoated tablet contains :
Loratadine	I.P.	10 mg
Excipients		q.s.
Approved Colour used

250

Citicoline Tablets I.P 500 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Citicoline Sodium (eq. to Citicoline)	I.P.	500 mg
Excipients		q.s.
Approved Colour used

251

Hydroxyzine Tablets I.P. 25 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Hydroxyzine Hydrochloride	I.P.	25 mg
Excipients		q.s.
Approved Colour used

252

Hydroxyzine Tablets I.P. 10 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Hydroxyzine Hydrochloride	I.P.	10 mg
Excipients		q.s.
Approved Colour used

253

Voglibose Tablets I.P. 0.3 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Voglibose	I.P.	0.3 mg
Excipients		q.s.
Approved Colour used

254

Voglibose Tablets I.P. 0.2 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Voglibose	I.P.	0.2 mg
Excipients		q.s.
Approved Colour used

255

Febuxostat Tablets 80 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Febuxostat		80 mg
Excipients		q.s.
Approved Colour used

256

Febuxostat Tablets 40 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Febuxostat		40 mg
Excipients		q.s.
Approved Colour used

257

Serratiopeptidase Tablets I.P. 10 mg

Composition	Standard	Quantity
Each enteric coated tablet contains :
Serratiopeptidase (as enteric coated granules eq. to enzymatic activity 20,000 units)	I.P.	10 mg
Excipients		q.s.
Approved Colour used

258

Paracetamol Tablets I.P. 650 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Paracetamol	I.P.	650 mg
Excipients		q.s.
Approved Colour used

259

Betahistine Hydrochloride Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Betahistine Hydrochloride	I.P.	8 mg
Excipients		q.s.
Approved Colour used

260

Betahistine Hydrochloride Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains :
Betahistine Hydrochloride	I.P.	16 mg
Excipients		q.s.
Approved Colour used

261

Levocetirizine Tablets I.P. 5 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Levocetirizine Hydrochloride	I.P.	5 mg
Excipients		q.s.
Approved Colour used

262

Cetirizine Hydrochloride Tablets I.P. 10 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Cetirizine Hydrochloride	I.P.	10 mg
Excipients		q.s.
Approved Colour used

263

Pantoprazole Gastro-resistant Tablets I.P. 40 mg

Composition	Standard	Quantity
Each enteric-coated tablet contains :
Pantoprazole Sodium eq. to Pantoprazole	I.P.	40 mg
Excipients		q.s.
Approved Colour used

264

Divalproex Extended Release Tablets I.P 1000mg

Composition	Standard	Quantity
Each film-coated extended-release tablet contains :
Divalproex Sodium eq. to Valproic Acid	I.P.	1000 mg
Excipients		q.s.
Approved Colour used

265

Divalproex Extended Release Tablets I.P 500mg

Composition	Standard	Quantity
Each film-coated extended-release tablet contains :
Divalproex Sodium eq. to Valproic Acid	I.P.	500 mg
Excipients		q.s.
Approved Colour used

266

Divalproex Extended Release Tablets I.P 250mg

Composition	Standard	Quantity
Each film-coated extended-release tablet contains :
Divalproex Sodium eq. to Valproic Acid	I.P.	250 mg
Excipients		q.s.
Approved Colour used

267

Telmisartan, Amlodipine and Hydrochlorothiazide Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Telmisartan	I.P.	40 mg
Amlodipine Besylate eq. to Amlodipine	I.P.	5 mg
Hydrochlorothiazide	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

268

Telmisartan 80 mg and Hydrochlorothiazide 12.5 mg Tablets I.P

Composition	Standard	Quantity
Each film-coated tablet contains :
Telmisartan	I.P.	80 mg
Hydrochlorothiazide	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

269

Telmisartan 40 mg and Hydrochlorothiazide 12.5 mg Tablets I.P.

Composition	Standard	Quantity
Each film-coated tablet contains :
Telmisartan	I.P.	40 mg
Hydrochlorothiazide	I.P.	12.5 mg
Excipients		q.s.
Approved Colour used

270

Telmisartan Tablets I.P. 80 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Telmisartan	I.P.	80 mg
Excipients		q.s.
Approved Colour used

271

Telmisartan Tablets I.P. 40 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Telmisartan	I.P.	40 mg
Excipients	q.s.
Approved Colour used

272

Telmisartan Tablets I.P. 20 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Telmisartan	I.P.	20 mg
Excipients		q.s.
Approved Colour used

273

Duloxetine Hydrochloride Tablets 30 mg

Composition	Standard	Quantity
Each enteric-coated tablet contains :
Duloxetine Hydrochloride eq. to Duloxetine	I.P.	30 mg
Excipients		q.s.
Approved Colour used

274

Duloxetine Hydrochloride Tablets 20mg

Composition	Standard	Quantity
Each enteric-coated tablet contains :
Duloxetine Hydrochloride eq. to Duloxetine	I.P.	20 mg
Excipients		q.s.
Approved Colour used

275

Rosuvastatin Calcium and Fenofibrate Tablets

Composition	Standard	Quantity
Each film-coated tablet contains :
Rosuvastatin Calcium eq. to Rosuvastatin	I.P.	10 mg
Fenofibrate	I.P.	160 mg
Excipients		q.s.
Colour

276

Rosuvastatin Calcium Tablets I.P. 20 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Rosuvastatin Calcium eq. to Rosuvastatin	I.P.	20 mg
Excipients		q.s.
Approved Colour used

277

Rosuvastatin Calcium Tablets I.P. 10 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Rosuvastatin Calcium eq. to Rosuvastatin	I.P.	10 mg
Excipients		q.s.
Approved Colour used

278

Rosuvastatin Calcium Tablets I.P. 5 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Rosuvastatin Calcium eq. to Rosuvastatin	I.P.	5 mg
Excipients		q.s.
Approved Colour used

279

Methylprednisolone Tablets I.P. 16 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Methylprednisolone	I.P.	16 mg
Excipients		q.s.
Approved Colour used

280

Methylprednisolone Tablets 8 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Methylprednisolone	I.P.	8 mg
Excipients		q.s.
Approved Colour used

281

Methylprednisolone Tablets I.P. 4 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Methylprednisolone	I.P.	4 mg
Excipients		q.s.
Approved Colour used

282

Atenolol Tablets I.P. 100 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Atenolol	I.P.	100 mg
Excipients		q.s.
Approved Colour used

283

Atenolol Tablets I.P. 50 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Atenolol	I.P.	50 mg
Excipients		q.s.
Approved Colour used

284

Atorvastatin Calcium and Fenofibrate Tablets

Composition	Standard	Quantity
Each film-coated tablet contains :
Atorvastatin Calcium eq. to Atorvastatin	I.P.	10 mg
Fenofibrate	I.P.	160 mg
Excipients		q.s.
Approved Colour used

285

Atorvastatin Tablets I.P. 40 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Atorvastatin Calcium eq. to Atorvastatin	I.P.	40 mg
Excipients		q.s.
Approved Colour used

286

Atorvastatin Tablets I.P. 20 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Atorvastatin Calcium eq. to Atorvastatin	I.P.	20 mg
Excipients		q.s.
Approved Colour used

287

Atorvastatin Tablets I.P. 10 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Atorvastatin Calcium eq. to Atorvastatin	I.P.	10 mg
Excipients		q.s.
Approved Colour used

288

Fexofenadine and Montelukast Tablets

Composition	Standard	Quantity
Each chewable film-coated tablet contains :
Fexofenadine Hydrochloride	I.P.	120 mg
Montelukast Sodium eq. to Montelukast	I.P.	10 mg
Excipients	q.s.
Approved Colour used

289

Fexofenadine Hydrochloride Tablets I.P. 180 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Fexofenadine Hydrochloride	I.P.	180 mg
Excipients	q.s.
Approved Colour used

290

Fexofenadine Hydrochloride Tablets I.P. 120 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Fexofenadine Hydrochloride	I.P.	120 mg
Excipients	q.s.
Approved Colour used

291

Escitalopram Tablets I.P 20 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Escitalopram Oxalate eq. to Escitalopram	I.P.	20 mg
Excipients	q.s.
Approved Colour used

292

Escitalopram Tablets I.P 10 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Escitalopram Oxalate eq. to Escitalopram	I.P.	10 mg
Excipients	q.s.
Approved Colour used

293

Escitalopram Tablets I.P 5 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Escitalopram Oxalate (eq. to Escitalopram)	I.P.	5 mg
Excipients	—	q.s.
Approved Colour used	—	—

294

Etoricoxib Tablets I.P 120 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Etoricoxib	I.P.	120 mg
Excipients	—	q.s.
Approved Colour used	—	—

295

Etoricoxib Tablets I.P 90 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Etoricoxib	I.P.	90 mg
Excipients	—	q.s.
Approved Colour used	—	—

296

Etoricoxib Tablets I.P 60 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Etoricoxib	I.P.	60 mg
Excipients	—	q.s.
Approved Colour used	—	—

297

Ondansetron Orally Disintegrating Tablets I.P. 8 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Ondansetron Hydrochloride (eq. to Ondansetron)	I.P.	8 mg
Excipients	—	q.s.
Approved Colour used	—	—

298

Ondansetron Orally Disintegrating Tablets I.P. 4 mg

Composition	Standard	Quantity
Each uncoated tablet contains :
Ondansetron Hydrochloride (eq. to Ondansetron)	I.P.	4 mg
Excipients	—	q.s.
Approved Colour used	—	—

299

Sildenafil Citrate Tablets I.P. 100 mg

Composition	Standard	Quantity
Each film-coated tablet contains :
Sildenafil Citrate (eq. to Sildenafil)	I.P.	100 mg
Excipients	—	q.s.
Approved Colour used	—	—

300

Paracetamol and Nimesulide Tablets (Not to be used for children below 12 years of age)

Composition	Standard	Quantity
Each uncoated tablet contains :
Paracetamol	I.P.	325 mg
Nimesulide	B.P.	100 mg
Excipients	—	q.s.
Approved Colour used	—	—

301

Roxithromycin Tablets I.P. 150 mg

Composition	Standard	Quantity
Each film coated tablet contains :
Roxithromycin	I.P.	150 mg
Excipients	—	q.s.
Approved Colour used	—	—

302

Deflazacort Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Deflazacort	—	30 mg
Excipients	—	q.s.
Approved Colour used	—	—

303

Deflazacort Tablets

Composition	Standard	Quantity
Each uncoated tablet contains :
Deflazacort	—	6 mg
Excipients	—	q.s.
Approved Colour used	—	—

304

Rabeprazole Gastro-resistant Tablets I.P. 20mg

Composition	Standard	Quantity
Each enteric coated tablet contains :
Rabeprazole Sodium	I.P.	20 mg
Excipients	—	q.s.
Approved Colour used	—	—

305

Ofloxacin & Ornidazole Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains :
Ofloxacin	I.P.	200 mg
Ornidazole	I.P.	500 mg
Excipients	—	q.s.
Approved Colour used	—	—

306

Levofloxacin Tablets I.P. 750 mg

Composition	Standard	Quantity
Each film coated tablet contains:
Levofloxacin Hemihydrate (eq. to Levofloxacin)	I.P.	750 mg
Excipients	—	q.s.
Approved Colour used	—	—

307

Levofloxacin Tablets I.P. 500 mg

Composition	Standard	Quantity
Each film coated tablet contains:
Levofloxacin Hemihydrate (eq. to Levofloxacin)	I.P.	500 mg
Excipients	—	q.s.
Approved Colour used	—	—

308

Levofloxacin Tablets I.P. 250 mg

Composition	Standard	Quantity
Each film coated tablet contains:
Levofloxacin Hemihydrate (eq. to Levofloxacin)	I.P.	250 mg
Excipients	—	q.s.
Approved Colour used	—	—

309

Pregabalin, Nortriptyline & Mecobalamin Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Pregabalin	I.P.	75 mg
Nortriptyline Hydrochloride (Eq. to Nortriptyline)	I.P.	10 mg
Mecobalamin	I.P.	1500 mcg
Excipients	—	q.s.
Approved Colour used	—	—

310

Azithromycin & Lactic Acid Bacillus Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Azithromycin Dihydrate (eq. to Azithromycin anhydrous)	I.P.	500 mg
Lactic Acid Bacillus	—	60 Million Spores
Excipients	—	q.s.
Approved Colour used	—	—

311

Ferrous Ascorbate, Cyanocobalamin, Folic Acid, Zinc Sulphate Monohydrate Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Ferrous Ascorbate	—	100 mg
Cyanocobalamin	I.P.	15 mcg
Folic Acid	I.P.	1.5 mg
Zinc Sulphate Monohydrate (eq. to Elemental Zinc)	I.P.	22.5 mg
Excipients	—	q.s.
Approved Colour used	—	—

312

Ofloxacin Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains:
Ofloxacin	I.P.	200 mg
Excipients	—	q.s.
Approved Colour used	—	—

313

Pregabalin (SR) and Methylcobalamin Tablets

Composition	Standard	Quantity
Each uncoated tablet contains:
Pregabalin (Sustained Release)	I.P.	75 mg
Methylcobalamin	I.P.	1500 mcg
Excipients	—	q.s.
Approved Colour used	—	—

314

Calcium Citrate, Zinc,Vitamin D3 and Magnesium Tablets

Composition	Standard	Quantity
Each uncoated tablet contains:
Calcium Citrate	USP	1000 mg
Zinc Sulphate Monohydrate eq. to Elemental Zinc	I.P.	4 mg
Vitamin D3	I.P.	200 IU
Magnesium Hydroxide eq. to Elemental Magnesium	I.P.	100 mg
Excipients	—	q.s.
Approved Colour used	—	—

315

Gabapentin and Methylcobalamin Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Gabapentin	I.P.	300 mg
Methylcobalamin	I.P.	500 mcg
Excipients	—	q.s.
Approved Colour used	—	—

316

Azithromycin Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains:
Azithromycin Dihydrate (eq. to Azithromycin Anhydrous)	I.P.	500 mg
Excipients	—	q.s.
Approved Colour used	—	—

317

Azithromycin Tablets I.P.

Composition	Standard	Quantity
Each film coated tablet contains:
Azithromycin Dihydrate (eq. to Azithromycin Anhydrous)	I.P.	250 mg
Excipients	—	q.s.
Approved Colour used	—	—

318

Ferrous Ascorbate, Folic acid and Zinc Sulphate Monohydrate Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Ferrous Ascorbate (eq. to Elemental Iron)	—	100 mg
Folic Acid	I.P.	1.5 mg
Zinc Sulphate Monohydrate (eq. to Elemental Zinc)	I.P.	22.5 mg
Excipients	—	q.s.
Approved Colour used	—	—

319

Aceclofenac, Paracetamol and Thiocolchicoside Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P.	100 mg
Paracetamol	I.P.	325 mg
Thiocolchicoside	I.P.	4 mg
Excipients	—	q.s.
Approved Colour used	—	—

320

Ursodeoxycholic Acid Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Ursodeoxycholic Acid	I.P.	300 mg
Excipients	—	q.s.
Approved Colour used	—	—

321

Aceclofenac, Paracetamol and Serratiopeptidase Tablets (Warning: Overdose of this drug has potential of severe liver injury & allergic reactions (e.g. swelling of face, mouth & throat, difficulty in breathing, itching or rashes)

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P.	100 mg
Paracetamol	I.P.	325 mg
Serratiopeptidase (eq. to enzymatic activity 20,000 units) (as enteric coated granules)	I.P.	10 mg
Excipients	—	q.s.
Approved Colour used	—	—

322

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P.	100 mg
Paracetamol	I.P.	325 mg
Serratiopeptidase (eq. to enzymatic activity 30,000 units) (as enteric coated granules)	I.P.	15 mg
Excipients	—	q.s.
Approved Colour used	—	—

323

Aceclofenac, Paracetamol and Chlorzoxazone Tablets (Warning: Overdose of this drug has potential of severe liver injury & allergic reactions (e.g. swelling of face, mouth & throat, difficulty in breathing, itching or rashes)

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P.	100 mg
Paracetamol	I.P.	325 mg
Chlorzoxazone	U.S.P.	250 mg
Excipients	—	q.s.
Approved Colour used	—	—

324

Aceclofenac and Paracetamol Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P.	100 mg
Paracetamol	I.P.	325 mg
Excipients	—	q.s.
Approved Colour used	—	—

325

Aceclofenac and Thiocolchicoside Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P.	100 mg
Thiocolchicoside	I.P.	4 mg
Excipients	—	q.s.
Approved Colour used	—	—

326

Telmisartan and Amlodipine Besilate Tablets I.P

Composition	Standard	Quantity
Each uncoated tablet contains:
Telmisartan	I.P.	40 mg
Amlodipine Besilate eq. to Amlodipine	I.P.	5 mg
Excipients	—	q.s.
Approved Colour used	—	—

327

Etoricoxib and Thiocolchicoside Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Etoricoxib	I.P.	60 mg
Thiocolchicoside	I.P.	4 mg
Excipients	—	q.s.
Approved Colour used	—	—

328

Montelukast and Levocetirizine Tablets I.P

Composition	Standard	Quantity
Each film coated tablet contains:
Montelukast Sodium eq. to Montelukast	I.P.	10 mg
Levocetirizine Hydrochloride	I.P.	5 mg
Excipients	—	q.s.
Approved Colour used	—	—

329

Alpha Lipoic Acid, Folic Acid, Methylcobalamin, Pyridoxine HCl and Vitamin D3 Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Alpha Lipoic Acid	USP	100 mg
Folic Acid	I.P	1.5 mg
Methylcobalamin	I.P	1500 mcg
Pyridoxine Hydrochloride	I.P	3 mg
Vitamin D3	I.P	1000 IU
Excipients	—	q.s.
Approved Colour used	—	—

330

Paracetamol, Phenylephrine HCl, Diphenhydramine HCl and Caffeine Tablets

Composition	Standard	Quantity
Each chewable film-coated tablet contains :
Fexofenadine Hydrochloride	I.P.	120 mg
Montelukast Sodium eq. to Montelukast	I.P.	10 mg
Excipients	q.s.
Approved Colour used

331

Levetiracetam Tablets I.P 500 mg

Composition	Standard	Quantity
Each film coated tablet contains:
Levetiracetam	I.P	500 mg
Excipients	—	q.s.
Approved colour used	—	—

332

Ketoconazole Tablets I.P 200mg

Composition	Standard	Quantity
Each film coated tablet contains:
Ketoconazole	I.P	200 mg
Excipients	—	q.s.
Approved colour used	—	—

333

Aceclofenac & Drotaverine HCl Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Aceclofenac	I.P	100 mg
Drotaverine Hydrochloride	I.P	80 mg
Excipients	—	q.s.
Approved Colour used	—	—

334

Etodolac and Paracetamol Tablets

Composition	Standard	Quantity
Each film coated tablet contains:
Etodolac	I.P	400 mg
Paracetamol	I.P	325 mg
Excipients	—	q.s.
Approved Colour used	—	—

335

Amisulpiride Tablets I.P 100 mg

Composition	Standard	Quantity
Each film coated tablet contains:
Amisulpride	I.P	100 mg
Excipients	—	q.s.
Approved colour used	—	—

336

Etodolac ER Tablets 400MG

Composition	Standard	Quantity
Each film coated extended release tablet contains:
Etodolac	I.P	400 mg
Excipients	—	q.s.
Approved Colour used	—	—

337

Nimesulide Tablets (Not to be used for children below 12 years of age)

Composition	Standard	Quantity
Each uncoated tablet contains :
Nimesulide	B.P.	100 mg
Excipients	q.s.
Approved Colour used

338

Methylcobalamin, Alpha Lipoic Acid, Inositol, Folic Acid, Chromium Polynicotinate, Selenium Dioxide and Benfotiamine Capsules

Ingredient	Standard	Quantity
Methylcobalamin	I.P	1500 mcg
Alpha Lipoic Acid	USP	100 mg
Inositol	USP	100 mg
Folic Acid	I.P	1.5 mg
Chromium Polynicotinate	USP	200 mcg
Selenium Dioxide	B.P	55 mcg
Benfotiamine	USP	150 mg
Excipients	—	q.s.
Approved colour used in empty capsule shells	—	—

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Krisa Healthcare is the most renowned organization in the country that offers a diverse range of healthcare items to its clients, covering all therapeutic areas. It implies that we meet every type of demand for healthcare items that are GMP and WHO-approved across many markets and also at very cost-efficient prices.

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