BACLOFEN - 16590-026-72 - (BACLOFEN)

Alphabetical Index


Drug Information of BACLOFEN

Product NDC: 16590-026
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: 16590-026
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072824
Marketing Category: ANDA
Start Marketing Date: 19910918

Package Information of BACLOFEN

Package NDC: 16590-026-72
Package Description: 120 TABLET in 1 BOTTLE (16590-026-72)

NDC Information of BACLOFEN

NDC Code 16590-026-72
Proprietary Name BACLOFEN
Package Description 120 TABLET in 1 BOTTLE (16590-026-72)
Product NDC 16590-026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BACLOFEN
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19910918
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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