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Zolpidem Tartrate - 76237-257-39 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 76237-257
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: 76237-257
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077322
Marketing Category: ANDA
Start Marketing Date: 20111020

Package Information of Zolpidem Tartrate

Package NDC: 76237-257-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (76237-257-39)

NDC Information of Zolpidem Tartrate

NDC Code 76237-257-39
Proprietary Name Zolpidem Tartrate
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (76237-257-39)
Product NDC 76237-257
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111020
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
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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