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Zolpidem tartrate
Zolpidem tartrate - 0904-6082-61 - (Zolpidem tartrate)
Drug Information of Zolpidem tartrate
| Product NDC: | 0904-6082 |
| 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) |
Labeler Information of Zolpidem tartrate
| Product NDC: | 0904-6082 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077903 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091102 |
Package Information of Zolpidem tartrate
| Package NDC: | 0904-6082-61 |
| Package Description: | 100 TABLET in 1 BOX, UNIT-DOSE (0904-6082-61) |
NDC Information of Zolpidem tartrate
| NDC Code | 0904-6082-61 |
| Proprietary Name | Zolpidem tartrate |
| Package Description | 100 TABLET in 1 BOX, UNIT-DOSE (0904-6082-61) |
| Product NDC | 0904-6082 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zolpidem tartrate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091102 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| 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] |
