Ambien - 21695-212-45 - (zolpidem tartrate)

Alphabetical Index


Drug Information of Ambien

Product NDC: 21695-212
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: 21695-212
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019908
Marketing Category: NDA
Start Marketing Date: 20090630

Package Information of Ambien

Package NDC: 21695-212-45
Package Description: 45 TABLET, FILM COATED in 1 BOTTLE (21695-212-45)

NDC Information of Ambien

NDC Code 21695-212-45
Proprietary Name Ambien
Package Description 45 TABLET, FILM COATED in 1 BOTTLE (21695-212-45)
Product NDC 21695-212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090630
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
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