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Zolpidem Tartrate - 60505-2604-8 - (zolpidem tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 60505-2604
Proprietary Name: Zolpidem Tartrate
Non Proprietary Name: zolpidem tartrate
Active Ingredient(s): 5    mg/1 & nbsp;   zolpidem tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Zolpidem Tartrate

Product NDC: 60505-2604
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077884
Marketing Category: ANDA
Start Marketing Date: 20070423

Package Information of Zolpidem Tartrate

Package NDC: 60505-2604-8
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2604-8)

NDC Information of Zolpidem Tartrate

NDC Code 60505-2604-8
Proprietary Name Zolpidem Tartrate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2604-8)
Product NDC 60505-2604
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070423
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name ZOLPIDEM TARTRATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [Chemical/Ingredient],Central Nervous System Depression [PE]

Complete Information of Zolpidem Tartrate


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