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Zolpidem tartrate - 60429-530-05 - (Zolpidem tartrate)

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Drug Information of Zolpidem tartrate

Product NDC: 60429-530
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: 60429-530
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078184
Marketing Category: ANDA
Start Marketing Date: 20080222

Package Information of Zolpidem tartrate

Package NDC: 60429-530-05
Package Description: 500 TABLET in 1 BOTTLE (60429-530-05)

NDC Information of Zolpidem tartrate

NDC Code 60429-530-05
Proprietary Name Zolpidem tartrate
Package Description 500 TABLET in 1 BOTTLE (60429-530-05)
Product NDC 60429-530
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080222
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
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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