Baclofen - 52959-677-30 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 52959-677
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: 52959-677
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072235
Marketing Category: ANDA
Start Marketing Date: 20100715

Package Information of Baclofen

Package NDC: 52959-677-30
Package Description: 30 TABLET in 1 BOTTLE (52959-677-30)

NDC Information of Baclofen

NDC Code 52959-677-30
Proprietary Name Baclofen
Package Description 30 TABLET in 1 BOTTLE (52959-677-30)
Product NDC 52959-677
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100715
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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