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Zolpidem Tartrate - 35356-745-90 - (zolpidem tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 35356-745
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: 35356-745
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077214
Marketing Category: ANDA
Start Marketing Date: 20070427

Package Information of Zolpidem Tartrate

Package NDC: 35356-745-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (35356-745-90)

NDC Information of Zolpidem Tartrate

NDC Code 35356-745-90
Proprietary Name Zolpidem Tartrate
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (35356-745-90)
Product NDC 35356-745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070427
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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