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Sumatriptan Succinate
Sumatriptan Succinate - 68084-339-97 - (sumatriptan succinate)
Drug Information of Sumatriptan Succinate
| Product NDC: | 68084-339 |
| 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, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sumatriptan Succinate
| Product NDC: | 68084-339 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076933 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130705 |
Package Information of Sumatriptan Succinate
| Package NDC: | 68084-339-97 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-339-97) > 9 TABLET, COATED in 1 BLISTER PACK (68084-339-96) |
NDC Information of Sumatriptan Succinate
| NDC Code | 68084-339-97 |
| Proprietary Name | Sumatriptan Succinate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-339-97) > 9 TABLET, COATED in 1 BLISTER PACK (68084-339-96) |
| Product NDC | 68084-339 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sumatriptan succinate |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130705 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| 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] |
