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Zolpidem
Zolpidem - 0143-9962-01 - (Zolpidem Tartrate)
Drug Information of Zolpidem
| Product NDC: | 0143-9962 |
| Proprietary Name: | Zolpidem |
| 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) |
Labeler Information of Zolpidem
| Product NDC: | 0143-9962 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078129 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080430 |
Package Information of Zolpidem
| Package NDC: | 0143-9962-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0143-9962-01) |
NDC Information of Zolpidem
| NDC Code | 0143-9962-01 |
| Proprietary Name | Zolpidem |
| Package Description | 100 TABLET in 1 BOTTLE (0143-9962-01) |
| Product NDC | 0143-9962 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zolpidem Tartrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080430 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| 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] |
