Baclofen - 0603-2406-02 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 0603-2406
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: 0603-2406
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077156
Marketing Category: ANDA
Start Marketing Date: 20050830

Package Information of Baclofen

Package NDC: 0603-2406-02
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (0603-2406-02)

NDC Information of Baclofen

NDC Code 0603-2406-02
Proprietary Name Baclofen
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (0603-2406-02)
Product NDC 0603-2406
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050830
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
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