Home
>
National Drug Code (NDC)
>
Zolpidem tartrate
Zolpidem tartrate - 0781-5315-31 - (Zolpidem tartrate)
Drug Information of Zolpidem tartrate
| Product NDC: | 0781-5315 |
| Proprietary Name: | Zolpidem tartrate |
| Non Proprietary Name: | Zolpidem tartrate |
| Active Ingredient(s): | 6.25 mg/1 & nbsp; Zolpidem tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zolpidem tartrate
| Product NDC: | 0781-5315 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090107 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111031 |
Package Information of Zolpidem tartrate
| Package NDC: | 0781-5315-31 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5315-31) |
NDC Information of Zolpidem tartrate
| NDC Code | 0781-5315-31 |
| Proprietary Name | Zolpidem tartrate |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5315-31) |
| Product NDC | 0781-5315 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zolpidem tartrate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20111031 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| 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] |
