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Sumatriptan Succinate
Sumatriptan Succinate - 0093-0222-90 - (Sumatriptan Succinate)
Drug Information of Sumatriptan Succinate
| Product NDC: | 0093-0222 |
| Proprietary Name: | Sumatriptan Succinate |
| Non Proprietary Name: | Sumatriptan Succinate |
| Active Ingredient(s): | 25 mg/1 & nbsp; Sumatriptan Succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumatriptan Succinate
| Product NDC: | 0093-0222 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076840 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090209 |
Package Information of Sumatriptan Succinate
| Package NDC: | 0093-0222-90 |
| Package Description: | 9 BLISTER PACK in 1 BOX (0093-0222-90) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-0222-19) |
NDC Information of Sumatriptan Succinate
| NDC Code | 0093-0222-90 |
| Proprietary Name | Sumatriptan Succinate |
| Package Description | 9 BLISTER PACK in 1 BOX (0093-0222-90) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-0222-19) |
| Product NDC | 0093-0222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sumatriptan Succinate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090209 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
