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Sumatriptan Succinate
Sumatriptan Succinate - 35356-438-09 - (Sumatriptan Succinate)
Drug Information of Sumatriptan Succinate
| Product NDC: | 35356-438 |
| Proprietary Name: | Sumatriptan Succinate |
| Non Proprietary Name: | Sumatriptan Succinate |
| Active Ingredient(s): | 100 mg/1 & nbsp; Sumatriptan Succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumatriptan Succinate
| Product NDC: | 35356-438 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076847 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091117 |
Package Information of Sumatriptan Succinate
| Package NDC: | 35356-438-09 |
| Package Description: | 9 BLISTER PACK in 1 CARTON (35356-438-09) > 9 TABLET in 1 BLISTER PACK |
NDC Information of Sumatriptan Succinate
| NDC Code | 35356-438-09 |
| Proprietary Name | Sumatriptan Succinate |
| Package Description | 9 BLISTER PACK in 1 CARTON (35356-438-09) > 9 TABLET in 1 BLISTER PACK |
| Product NDC | 35356-438 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sumatriptan Succinate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091117 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
