Baclofen - 63739-031-01 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 63739-031
Proprietary Name: Baclofen
Non Proprietary Name: Baclofen
Active Ingredient(s): 10    mg/1 & nbsp;   Baclofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Baclofen

Product NDC: 63739-031
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072824
Marketing Category: ANDA
Start Marketing Date: 20040701

Package Information of Baclofen

Package NDC: 63739-031-01
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-031-01) > 30 TABLET in 1 BLISTER PACK

NDC Information of Baclofen

NDC Code 63739-031-01
Proprietary Name Baclofen
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-031-01) > 30 TABLET in 1 BLISTER PACK
Product NDC 63739-031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040701
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name BACLOFEN
Strength Number 10
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