GABITRIL - 16590-832-30 - (TIAGABINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of GABITRIL

Product NDC: 16590-832
Proprietary Name: GABITRIL
Non Proprietary Name: TIAGABINE HYDROCHLORIDE
Active Ingredient(s): 12    mg/1 & nbsp;   TIAGABINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of GABITRIL

Product NDC: 16590-832
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020646
Marketing Category: NDA
Start Marketing Date: 19971103

Package Information of GABITRIL

Package NDC: 16590-832-30
Package Description: 30 TABLET in 1 BOTTLE (16590-832-30)

NDC Information of GABITRIL

NDC Code 16590-832-30
Proprietary Name GABITRIL
Package Description 30 TABLET in 1 BOTTLE (16590-832-30)
Product NDC 16590-832
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TIAGABINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19971103
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
Substance Name TIAGABINE HYDROCHLORIDE
Strength Number 12
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of GABITRIL


General Information