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Zolpidem Tartrate - 0781-5318-31 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 0781-5318
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Zolpidem Tartrate

Product NDC: 0781-5318
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077322
Marketing Category: ANDA
Start Marketing Date: 20070423

Package Information of Zolpidem Tartrate

Package NDC: 0781-5318-31
Package Description: 30 TABLET, COATED in 1 BOTTLE (0781-5318-31)

NDC Information of Zolpidem Tartrate

NDC Code 0781-5318-31
Proprietary Name Zolpidem Tartrate
Package Description 30 TABLET, COATED in 1 BOTTLE (0781-5318-31)
Product NDC 0781-5318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20070423
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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