Baclofen - 0615-3542-31 - (Baclofen)

Alphabetical Index


Drug Information of Baclofen

Product NDC: 0615-3542
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: 0615-3542
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072235
Marketing Category: ANDA
Start Marketing Date: 20100715

Package Information of Baclofen

Package NDC: 0615-3542-31
Package Description: 31 TABLET in 1 BLISTER PACK (0615-3542-31)

NDC Information of Baclofen

NDC Code 0615-3542-31
Proprietary Name Baclofen
Package Description 31 TABLET in 1 BLISTER PACK (0615-3542-31)
Product NDC 0615-3542
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100715
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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