Baclofen - 0904-5222-61 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 0904-5222
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: 0904-5222
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072235
Marketing Category: ANDA
Start Marketing Date: 19980721

Package Information of Baclofen

Package NDC: 0904-5222-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-5222-61)

NDC Information of Baclofen

NDC Code 0904-5222-61
Proprietary Name Baclofen
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-5222-61)
Product NDC 0904-5222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980721
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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