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Zolpidem Tartrate - 61442-232-05 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 61442-232
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: 61442-232
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077990
Marketing Category: ANDA
Start Marketing Date: 20070423

Package Information of Zolpidem Tartrate

Package NDC: 61442-232-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (61442-232-05)

NDC Information of Zolpidem Tartrate

NDC Code 61442-232-05
Proprietary Name Zolpidem Tartrate
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (61442-232-05)
Product NDC 61442-232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070423
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
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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