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Sumatriptan Succinate
Sumatriptan Succinate - 55390-325-02 - (Sumatriptan Succinate)
Drug Information of Sumatriptan Succinate
| Product NDC: | 55390-325 |
| 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, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumatriptan Succinate
| Product NDC: | 55390-325 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090310 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101203 |
Package Information of Sumatriptan Succinate
| Package NDC: | 55390-325-02 |
| Package Description: | 2 SYRINGE in 1 BOX (55390-325-02) > .5 mL in 1 SYRINGE |
NDC Information of Sumatriptan Succinate
| NDC Code | 55390-325-02 |
| Proprietary Name | Sumatriptan Succinate |
| Package Description | 2 SYRINGE in 1 BOX (55390-325-02) > .5 mL in 1 SYRINGE |
| Product NDC | 55390-325 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sumatriptan Succinate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20101203 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| 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] |
