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Zolpidem Tartrate - 65862-160-99 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 65862-160
Proprietary Name: Zolpidem Tartrate
Non Proprietary Name: Zolpidem Tartrate
Active Ingredient(s): 10    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: 65862-160
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078413
Marketing Category: ANDA
Start Marketing Date: 20070504

Package Information of Zolpidem Tartrate

Package NDC: 65862-160-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-160-99)

NDC Information of Zolpidem Tartrate

NDC Code 65862-160-99
Proprietary Name Zolpidem Tartrate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (65862-160-99)
Product NDC 65862-160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070504
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name ZOLPIDEM TARTRATE
Strength Number 10
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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