Baclofen - 68788-9735-3 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 68788-9735
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: 68788-9735
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077156
Marketing Category: ANDA
Start Marketing Date: 20120430

Package Information of Baclofen

Package NDC: 68788-9735-3
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68788-9735-3)

NDC Information of Baclofen

NDC Code 68788-9735-3
Proprietary Name Baclofen
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68788-9735-3)
Product NDC 68788-9735
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120430
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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