Baclofen - 68788-0522-1 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 68788-0522
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: 68788-0522
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072824
Marketing Category: ANDA
Start Marketing Date: 20040701

Package Information of Baclofen

Package NDC: 68788-0522-1
Package Description: 100 TABLET in 1 BOTTLE (68788-0522-1)

NDC Information of Baclofen

NDC Code 68788-0522-1
Proprietary Name Baclofen
Package Description 100 TABLET in 1 BOTTLE (68788-0522-1)
Product NDC 68788-0522
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 Preferred Pharmaceuticals, Inc
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