Baclofen - 16714-071-02 - (Baclofen)

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Drug Information of Baclofen

Product NDC: 16714-071
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: 16714-071
Labeler Name: Northstar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078504
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Baclofen

Package NDC: 16714-071-02
Package Description: 60 TABLET in 1 BOTTLE (16714-071-02)

NDC Information of Baclofen

NDC Code 16714-071-02
Proprietary Name Baclofen
Package Description 60 TABLET in 1 BOTTLE (16714-071-02)
Product NDC 16714-071
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Northstar RxLLC
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