Home > National Drug Code (NDC) > TIAGABINE HYDROCHLORIDE

TIAGABINE HYDROCHLORIDE - 62756-200-83 - (TIAGABINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of TIAGABINE HYDROCHLORIDE

Product NDC: 62756-200
Proprietary Name: TIAGABINE HYDROCHLORIDE
Non Proprietary Name: TIAGABINE HYDROCHLORIDE
Active Ingredient(s): 2    mg/1 & nbsp;   TIAGABINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TIAGABINE HYDROCHLORIDE

Product NDC: 62756-200
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077555
Marketing Category: ANDA
Start Marketing Date: 20111104

Package Information of TIAGABINE HYDROCHLORIDE

Package NDC: 62756-200-83
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (62756-200-83)

NDC Information of TIAGABINE HYDROCHLORIDE

NDC Code 62756-200-83
Proprietary Name TIAGABINE HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (62756-200-83)
Product NDC 62756-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TIAGABINE HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111104
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name TIAGABINE HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of TIAGABINE HYDROCHLORIDE


General Information