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ZOLPIDEM TARTRATE - 55154-2069-0 - (ZOLPIDEM TARTRATE)

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Drug Information of ZOLPIDEM TARTRATE

Product NDC: 55154-2069
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
Coding System: National Drug Codes(NDC)

Labeler Information of ZOLPIDEM TARTRATE

Product NDC: 55154-2069
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078426
Marketing Category: ANDA
Start Marketing Date: 20091014

Package Information of ZOLPIDEM TARTRATE

Package NDC: 55154-2069-0
Package Description: 1 BLISTER PACK in 1 BAG (55154-2069-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of ZOLPIDEM TARTRATE

NDC Code 55154-2069-0
Proprietary Name ZOLPIDEM TARTRATE
Package Description 1 BLISTER PACK in 1 BAG (55154-2069-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 55154-2069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ZOLPIDEM TARTRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091014
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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