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Zolpidem Tartrate - 10370-117-00 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 10370-117
Proprietary Name: Zolpidem Tartrate
Non Proprietary Name: Zolpidem Tartrate
Active Ingredient(s): 6.25    mg/1 & nbsp;   Zolpidem Tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Zolpidem Tartrate

Product NDC: 10370-117
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078148
Marketing Category: ANDA
Start Marketing Date: 20110414

Package Information of Zolpidem Tartrate

Package NDC: 10370-117-00
Package Description: 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-117-00)

NDC Information of Zolpidem Tartrate

NDC Code 10370-117-00
Proprietary Name Zolpidem Tartrate
Package Description 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-117-00)
Product NDC 10370-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110414
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, Inc.
Substance Name ZOLPIDEM TARTRATE
Strength Number 6.25
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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