Baclofen - 49349-787-02 - (Baclofen)

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Drug Information of Baclofen

Product NDC: 49349-787
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: 49349-787
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077156
Marketing Category: ANDA
Start Marketing Date: 20111010

Package Information of Baclofen

Package NDC: 49349-787-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-787-02)

NDC Information of Baclofen

NDC Code 49349-787-02
Proprietary Name Baclofen
Package Description 30 TABLET in 1 BLISTER PACK (49349-787-02)
Product NDC 49349-787
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111010
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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