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ZOLPIDEM TARTRATE - 13668-008-10 - (zolpidem tartrate)

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Drug Information of ZOLPIDEM TARTRATE

Product NDC: 13668-008
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: 13668-008
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077903
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of ZOLPIDEM TARTRATE

Package NDC: 13668-008-10
Package Description: 1000 TABLET in 1 BOTTLE (13668-008-10)

NDC Information of ZOLPIDEM TARTRATE

NDC Code 13668-008-10
Proprietary Name ZOLPIDEM TARTRATE
Package Description 1000 TABLET in 1 BOTTLE (13668-008-10)
Product NDC 13668-008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070905
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
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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