Baclofen - 63629-3193-7 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 63629-3193
Proprietary Name: Baclofen
Non Proprietary Name: Baclofen
Active Ingredient(s): 20    mg/1 & nbsp;   Baclofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Baclofen

Product NDC: 63629-3193
Labeler Name: Bryant Ranch Rrepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077241
Marketing Category: ANDA
Start Marketing Date: 20070701

Package Information of Baclofen

Package NDC: 63629-3193-7
Package Description: 56 TABLET in 1 BOTTLE, PLASTIC (63629-3193-7)

NDC Information of Baclofen

NDC Code 63629-3193-7
Proprietary Name Baclofen
Package Description 56 TABLET in 1 BOTTLE, PLASTIC (63629-3193-7)
Product NDC 63629-3193
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070701
Marketing Category Name ANDA
Labeler Name Bryant Ranch Rrepack
Substance Name BACLOFEN
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes GABA A Agonists [MoA],GABA B Agonists [MoA],gamma-Aminobutyric Acid-ergic Agonist [EPC]

Complete Information of Baclofen


General Information