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zolmiptriptan
zolmiptriptan - 68462-500-33 - (zolmitriptan)
Drug Information of zolmiptriptan
| Product NDC: | 68462-500 |
| Proprietary Name: | zolmiptriptan |
| 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 zolmiptriptan
| Product NDC: | 68462-500 |
| Labeler Name: | Glenmark Generics Inc.,USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202560 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130514 |
Package Information of zolmiptriptan
| Package NDC: | 68462-500-33 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (68462-500-33) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of zolmiptriptan
| NDC Code | 68462-500-33 |
| Proprietary Name | zolmiptriptan |
| Package Description | 1 BLISTER PACK in 1 CARTON (68462-500-33) > 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 68462-500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | zolmitriptan |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20130514 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc.,USA |
| 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] |
