Baclofen - 58118-1024-0 - (Baclofen)

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Drug Information of Baclofen

Product NDC: 58118-1024
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: 58118-1024
Labeler Name: Clinical Solutions Wholesale
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074584
Marketing Category: ANDA
Start Marketing Date: 20101020

Package Information of Baclofen

Package NDC: 58118-1024-0
Package Description: 1 TABLET in 1 PACKET (58118-1024-0)

NDC Information of Baclofen

NDC Code 58118-1024-0
Proprietary Name Baclofen
Package Description 1 TABLET in 1 PACKET (58118-1024-0)
Product NDC 58118-1024
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101020
Marketing Category Name ANDA
Labeler Name Clinical Solutions Wholesale
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