Product NDC: | 63629-3548 |
Proprietary Name: | Zolpidem Tartrate |
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: | 63629-3548 |
Labeler Name: | Bryant Ranch Prepack |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078616 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081121 |
Package NDC: | 63629-3548-7 |
Package Description: | 15 TABLET, FILM COATED in 1 BOTTLE (63629-3548-7) |
NDC Code | 63629-3548-7 |
Proprietary Name | Zolpidem Tartrate |
Package Description | 15 TABLET, FILM COATED in 1 BOTTLE (63629-3548-7) |
Product NDC | 63629-3548 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | zolpidem tartrate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20081121 |
Marketing Category Name | ANDA |
Labeler Name | Bryant Ranch Prepack |
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] |