Baclofen - 21695-014-72 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 21695-014
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: 21695-014
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072824
Marketing Category: ANDA
Start Marketing Date: 20040701

Package Information of Baclofen

Package NDC: 21695-014-72
Package Description: 120 TABLET in 1 BOTTLE (21695-014-72)

NDC Information of Baclofen

NDC Code 21695-014-72
Proprietary Name Baclofen
Package Description 120 TABLET in 1 BOTTLE (21695-014-72)
Product NDC 21695-014
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 Rebel Distributors Corp.
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