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Sumatriptan
Sumatriptan - 59762-1851-9 - (Sumatriptan Succinate)
Drug Information of Sumatriptan
| Product NDC: | 59762-1851 |
| Proprietary Name: | Sumatriptan |
| Non Proprietary Name: | Sumatriptan Succinate |
| Active Ingredient(s): | 50 mg/1 & nbsp; Sumatriptan Succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumatriptan
| Product NDC: | 59762-1851 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078327 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090817 |
Package Information of Sumatriptan
| Package NDC: | 59762-1851-9 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59762-1851-9) > 9 TABLET in 1 BLISTER PACK (59762-1851-3) |
NDC Information of Sumatriptan
| NDC Code | 59762-1851-9 |
| Proprietary Name | Sumatriptan |
| Package Description | 1 BLISTER PACK in 1 CARTON (59762-1851-9) > 9 TABLET in 1 BLISTER PACK (59762-1851-3) |
| Product NDC | 59762-1851 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sumatriptan Succinate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090817 |
| Marketing Category Name | ANDA |
| Labeler Name | Greenstone LLC |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
