Home > National Drug Code (NDC) > ZOLPIDEM TARTRATE

ZOLPIDEM TARTRATE - 55648-715-04 - (zolpidem tartrate)

Alphabetical Index


Drug Information of ZOLPIDEM TARTRATE

Product NDC: 55648-715
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZOLPIDEM TARTRATE

Product NDC: 55648-715
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078426
Marketing Category: ANDA
Start Marketing Date: 20070515

Package Information of ZOLPIDEM TARTRATE

Package NDC: 55648-715-04
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (55648-715-04)

NDC Information of ZOLPIDEM TARTRATE

NDC Code 55648-715-04
Proprietary Name ZOLPIDEM TARTRATE
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (55648-715-04)
Product NDC 55648-715
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070515
Marketing Category Name ANDA
Labeler Name Wockhardt 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


General Information