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ZOLPIDEM TARTRATE - 68084-226-01 - (ZOLPIDEM TARTRATE)

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Drug Information of ZOLPIDEM TARTRATE

Product NDC: 68084-226
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
Coding System: National Drug Codes(NDC)

Labeler Information of ZOLPIDEM TARTRATE

Product NDC: 68084-226
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078426
Marketing Category: ANDA
Start Marketing Date: 20091014

Package Information of ZOLPIDEM TARTRATE

Package NDC: 68084-226-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-226-01) > 10 TABLET in 1 BLISTER PACK (68084-226-11)

NDC Information of ZOLPIDEM TARTRATE

NDC Code 68084-226-01
Proprietary Name ZOLPIDEM TARTRATE
Package Description 10 BLISTER PACK in 1 CARTON (68084-226-01) > 10 TABLET in 1 BLISTER PACK (68084-226-11)
Product NDC 68084-226
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 American Health Packaging
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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