Ambien - 54569-5760-1 - (zolpidem tartrate)

Alphabetical Index


Drug Information of Ambien

Product NDC: 54569-5760
Proprietary Name: Ambien
Non Proprietary Name: zolpidem tartrate
Active Ingredient(s): 12.5    mg/1 & nbsp;   zolpidem tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ambien

Product NDC: 54569-5760
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021774
Marketing Category: NDA
Start Marketing Date: 20050919

Package Information of Ambien

Package NDC: 54569-5760-1
Package Description: 20 TABLET, COATED in 1 BOTTLE (54569-5760-1)

NDC Information of Ambien

NDC Code 54569-5760-1
Proprietary Name Ambien
Package Description 20 TABLET, COATED in 1 BOTTLE (54569-5760-1)
Product NDC 54569-5760
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20050919
Marketing Category Name NDA
Labeler Name A-S Medication Solutions LLC
Substance Name ZOLPIDEM TARTRATE
Strength Number 12.5
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 Ambien


General Information