Zolpidem - 0143-9963-05 - (Zolpidem Tartrate)

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Drug Information of Zolpidem

Product NDC: 0143-9963
Proprietary Name: Zolpidem
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

Product NDC: 0143-9963
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078129
Marketing Category: ANDA
Start Marketing Date: 20080430

Package Information of Zolpidem

Package NDC: 0143-9963-05
Package Description: 500 TABLET in 1 BOTTLE (0143-9963-05)

NDC Information of Zolpidem

NDC Code 0143-9963-05
Proprietary Name Zolpidem
Package Description 500 TABLET in 1 BOTTLE (0143-9963-05)
Product NDC 0143-9963
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080430
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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


General Information