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Zolmitriptan
Zolmitriptan - 68382-717-82 - (Zolmitriptan)
Drug Information of Zolmitriptan
| Product NDC: | 68382-717 |
| Proprietary Name: | Zolmitriptan |
| Non Proprietary Name: | Zolmitriptan |
| Active Ingredient(s): | 5 mg/1 & nbsp; Zolmitriptan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zolmitriptan
| Product NDC: | 68382-717 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202890 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130516 |
Package Information of Zolmitriptan
| Package NDC: | 68382-717-82 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (68382-717-82) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-717-87) |
NDC Information of Zolmitriptan
| NDC Code | 68382-717-82 |
| Proprietary Name | Zolmitriptan |
| Package Description | 1 BLISTER PACK in 1 CARTON (68382-717-82) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-717-87) |
| Product NDC | 68382-717 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Zolmitriptan |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20130516 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | ZOLMITRIPTAN |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
