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Zolpidem Tartrate - 68788-9904-3 - (zolpidem tartrate)

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Drug Information of Zolpidem Tartrate

Product NDC: 68788-9904
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: 68788-9904
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078616
Marketing Category: ANDA
Start Marketing Date: 20120130

Package Information of Zolpidem Tartrate

Package NDC: 68788-9904-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-9904-3)

NDC Information of Zolpidem Tartrate

NDC Code 68788-9904-3
Proprietary Name Zolpidem Tartrate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-9904-3)
Product NDC 68788-9904
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120130
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
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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