Baclofen - 0832-1025-50 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 0832-1025
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: 0832-1025
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074584
Marketing Category: ANDA
Start Marketing Date: 20101020

Package Information of Baclofen

Package NDC: 0832-1025-50
Package Description: 500 TABLET in 1 BOTTLE (0832-1025-50)

NDC Information of Baclofen

NDC Code 0832-1025-50
Proprietary Name Baclofen
Package Description 500 TABLET in 1 BOTTLE (0832-1025-50)
Product NDC 0832-1025
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101020
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
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