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Zolpidem Tartrate - 0955-1703-10 - (zolpidem tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 0955-1703
Proprietary Name: Zolpidem Tartrate
Non Proprietary Name: zolpidem tartrate
Active Ingredient(s): 12.5    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: 0955-1703
Labeler Name: Winthrop U.S, a business of sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021774
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20101206

Package Information of Zolpidem Tartrate

Package NDC: 0955-1703-10
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0955-1703-10)

NDC Information of Zolpidem Tartrate

NDC Code 0955-1703-10
Proprietary Name Zolpidem Tartrate
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0955-1703-10)
Product NDC 0955-1703
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 20101206
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Winthrop U.S, a business of sanofi-aventis U.S. LLC
Substance Name ZOLPIDEM TARTRATE
Strength Number 12.5
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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