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Zolpidem Tartrate - 16714-621-11 - (Zolpidem Tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 16714-621
Proprietary Name: Zolpidem Tartrate
Non Proprietary Name: Zolpidem Tartrate
Active Ingredient(s): 5    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: 16714-621
Labeler Name: NorthStar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078413
Marketing Category: ANDA
Start Marketing Date: 20070504

Package Information of Zolpidem Tartrate

Package NDC: 16714-621-11
Package Description: 10 BLISTER PACK in 1 CARTON (16714-621-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-621-10)

NDC Information of Zolpidem Tartrate

NDC Code 16714-621-11
Proprietary Name Zolpidem Tartrate
Package Description 10 BLISTER PACK in 1 CARTON (16714-621-11) > 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-621-10)
Product NDC 16714-621
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zolpidem Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070504
Marketing Category Name ANDA
Labeler Name NorthStar Rx LLC
Substance Name ZOLPIDEM TARTRATE
Strength Number 5
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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