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NARATRIPTAN HYDROCHLORIDE - 62756-437-69 - (NARATRIPTAN HYDROCHLORIDE)

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Drug Information of NARATRIPTAN HYDROCHLORIDE

Product NDC: 62756-437
Proprietary Name: NARATRIPTAN HYDROCHLORIDE
Non Proprietary Name: NARATRIPTAN HYDROCHLORIDE
Active Ingredient(s): 2.5    mg/1 & nbsp;   NARATRIPTAN HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of NARATRIPTAN HYDROCHLORIDE

Product NDC: 62756-437
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091552
Marketing Category: ANDA
Start Marketing Date: 20110222

Package Information of NARATRIPTAN HYDROCHLORIDE

Package NDC: 62756-437-69
Package Description: 1 BLISTER PACK in 1 CARTON (62756-437-69) > 9 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of NARATRIPTAN HYDROCHLORIDE

NDC Code 62756-437-69
Proprietary Name NARATRIPTAN HYDROCHLORIDE
Package Description 1 BLISTER PACK in 1 CARTON (62756-437-69) > 9 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 62756-437
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NARATRIPTAN HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110222
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name NARATRIPTAN HYDROCHLORIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]

Complete Information of NARATRIPTAN HYDROCHLORIDE


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