Ambien CR - 21695-213-30 - (zolpidem tartrate)

Alphabetical Index


Drug Information of Ambien CR

Product NDC: 21695-213
Proprietary Name: Ambien CR
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 CR

Product NDC: 21695-213
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021774
Marketing Category: NDA
Start Marketing Date: 20090630

Package Information of Ambien CR

Package NDC: 21695-213-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (21695-213-30)

NDC Information of Ambien CR

NDC Code 21695-213-30
Proprietary Name Ambien CR
Package Description 30 TABLET, COATED in 1 BOTTLE (21695-213-30)
Product NDC 21695-213
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20090630
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
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 CR


General Information