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SUMATRIPTAN SUCCINATE
SUMATRIPTAN SUCCINATE - 0781-3169-07 - (sumatriptan succinate)
Drug Information of SUMATRIPTAN SUCCINATE
| Product NDC: | 0781-3169 |
| Proprietary Name: | SUMATRIPTAN SUCCINATE |
| Non Proprietary Name: | sumatriptan succinate |
| Active Ingredient(s): | 4 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: | 0781-3169 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020080 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120112 |
Package Information of SUMATRIPTAN SUCCINATE
| Package NDC: | 0781-3169-07 |
| Package Description: | 1 PACKAGE in 1 CARTON (0781-3169-07) > 2 SYRINGE in 1 PACKAGE > .5 mL in 1 SYRINGE |
NDC Information of SUMATRIPTAN SUCCINATE
| NDC Code | 0781-3169-07 |
| Proprietary Name | SUMATRIPTAN SUCCINATE |
| Package Description | 1 PACKAGE in 1 CARTON (0781-3169-07) > 2 SYRINGE in 1 PACKAGE > .5 mL in 1 SYRINGE |
| Product NDC | 0781-3169 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sumatriptan succinate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20120112 |
| Marketing Category Name | NDA |
| Labeler Name | Sandoz Inc |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Strength Number | 4 |
| Strength Unit | mg/.5mL |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
