Product NDC: | 67296-0759 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67296-0759 |
Labeler Name: | RedPharm Drug Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078616 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081121 |
Package NDC: | 67296-0759-1 |
Package Description: | 30 TABLET in 1 BOTTLE (67296-0759-1) |
NDC Code | 67296-0759-1 |
Proprietary Name | Zolpidem Tartrate |
Package Description | 30 TABLET in 1 BOTTLE (67296-0759-1) |
Product NDC | 67296-0759 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Zolpidem Tartrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20081121 |
Marketing Category Name | ANDA |
Labeler Name | RedPharm Drug Inc. |
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] |