Product NDC: | 13668-007 |
Proprietary Name: | ZOLPIDEM TARTRATE |
Non Proprietary Name: | zolpidem tartrate |
Active Ingredient(s): | 5 mg/1 & nbsp; zolpidem tartrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13668-007 |
Labeler Name: | Torrent Pharmaceuticals Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077903 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070905 |
Package NDC: | 13668-007-74 |
Package Description: | 100 TABLET in 1 CARTON (13668-007-74) |
NDC Code | 13668-007-74 |
Proprietary Name | ZOLPIDEM TARTRATE |
Package Description | 100 TABLET in 1 CARTON (13668-007-74) |
Product NDC | 13668-007 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | zolpidem tartrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070905 |
Marketing Category Name | ANDA |
Labeler Name | Torrent Pharmaceuticals Limited |
Substance Name | ZOLPIDEM TARTRATE |
Strength Number | 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] |