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Sumatriptan Succinate
Sumatriptan Succinate - 0703-7351-02 - (Sumatriptan Succinate)
Drug Information of Sumatriptan Succinate
| Product NDC: | 0703-7351 |
| Proprietary Name: | Sumatriptan Succinate |
| Non Proprietary Name: | Sumatriptan Succinate |
| Active Ingredient(s): | 6 mg/.5mL & nbsp; Sumatriptan Succinate |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumatriptan Succinate
| Product NDC: | 0703-7351 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077907 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090206 |
Package Information of Sumatriptan Succinate
| Package NDC: | 0703-7351-02 |
| Package Description: | 5 VIAL, SINGLE-DOSE in 1 CARTON (0703-7351-02) > .5 mL in 1 VIAL, SINGLE-DOSE (0703-7351-01) |
NDC Information of Sumatriptan Succinate
| NDC Code | 0703-7351-02 |
| Proprietary Name | Sumatriptan Succinate |
| Package Description | 5 VIAL, SINGLE-DOSE in 1 CARTON (0703-7351-02) > .5 mL in 1 VIAL, SINGLE-DOSE (0703-7351-01) |
| Product NDC | 0703-7351 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sumatriptan Succinate |
| Dosage Form Name | INJECTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090206 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Strength Number | 6 |
| Strength Unit | mg/.5mL |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
