Ambien - 49999-764-30 - (zolpidem tartrate)

Alphabetical Index


Drug Information of Ambien

Product NDC: 49999-764
Proprietary Name: Ambien
Non Proprietary Name: zolpidem tartrate
Active Ingredient(s): 6.25    mg/1 & nbsp;   zolpidem tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ambien

Product NDC: 49999-764
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021774
Marketing Category: NDA
Start Marketing Date: 20111110

Package Information of Ambien

Package NDC: 49999-764-30
Package Description: 30 TABLET in 1 BOTTLE (49999-764-30)

NDC Information of Ambien

NDC Code 49999-764-30
Proprietary Name Ambien
Package Description 30 TABLET in 1 BOTTLE (49999-764-30)
Product NDC 49999-764
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zolpidem tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111110
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ZOLPIDEM TARTRATE
Strength Number 6.25
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