Product NDC: | 16590-010 |
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) |
Product NDC: | 16590-010 |
Labeler Name: | STAT Rx USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019908 |
Marketing Category: | NDA |
Start Marketing Date: | 19930401 |
Package NDC: | 16590-010-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (16590-010-30) |
NDC Code | 16590-010-30 |
Proprietary Name | AMBIEN |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (16590-010-30) |
Product NDC | 16590-010 |
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 | STAT Rx USA 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] |