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Zolpidem Tartrate - 0179-1980-15 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 0179-1980
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Zolpidem Tartrate

Product NDC: 0179-1980
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA077322
Marketing Category: NDA
Start Marketing Date: 20081001

Package Information of Zolpidem Tartrate

Package NDC: 0179-1980-15
Package Description: 15 TABLET, COATED in 1 BOTTLE (0179-1980-15)

NDC Information of Zolpidem Tartrate

NDC Code 0179-1980-15
Proprietary Name Zolpidem Tartrate
Package Description 15 TABLET, COATED in 1 BOTTLE (0179-1980-15)
Product NDC 0179-1980
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20081001
Marketing Category Name NDA
Labeler Name KAISER FOUNDATION HOSPITALS
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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