GABITRIL - 49999-692-60 - (tiagabine hydrochloride)

Alphabetical Index


Drug Information of GABITRIL

Product NDC: 49999-692
Proprietary Name: GABITRIL
Non Proprietary Name: tiagabine hydrochloride
Active Ingredient(s): 4    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: 49999-692
Labeler Name: Lake Erie Medical & Surgial Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020646
Marketing Category: NDA
Start Marketing Date: 20111115

Package Information of GABITRIL

Package NDC: 49999-692-60
Package Description: 60 TABLET in 1 BOTTLE (49999-692-60)

NDC Information of GABITRIL

NDC Code 49999-692-60
Proprietary Name GABITRIL
Package Description 60 TABLET in 1 BOTTLE (49999-692-60)
Product NDC 49999-692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tiagabine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111115
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgial Supply DBA Quality Care Products LLC
Substance Name TIAGABINE HYDROCHLORIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of GABITRIL


General Information