Ambien - 0024-5421-50 - (zolpidem tartrate)

Alphabetical Index


Drug Information of Ambien

Product NDC: 0024-5421
Proprietary Name: Ambien
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 Ambien

Product NDC: 0024-5421
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019908
Marketing Category: NDA
Start Marketing Date: 19930401

Package Information of Ambien

Package NDC: 0024-5421-50
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0024-5421-50)

NDC Information of Ambien

NDC Code 0024-5421-50
Proprietary Name Ambien
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0024-5421-50)
Product NDC 0024-5421
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19930401
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. 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 Ambien


General Information