Baclofen - 49999-691-90 - (Baclofen)

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Drug Information of Baclofen

Product NDC: 49999-691
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: 49999-691
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072825
Marketing Category: ANDA
Start Marketing Date: 20101115

Package Information of Baclofen

Package NDC: 49999-691-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (49999-691-90)

NDC Information of Baclofen

NDC Code 49999-691-90
Proprietary Name Baclofen
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (49999-691-90)
Product NDC 49999-691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Baclofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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