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SUMATRIPTAN
SUMATRIPTAN - 0781-6524-86 - (sumatriptan)
Drug Information of SUMATRIPTAN
| Product NDC: | 0781-6524 |
| Proprietary Name: | SUMATRIPTAN |
| Non Proprietary Name: | sumatriptan |
| Active Ingredient(s): | 5 mg/100uL & nbsp; sumatriptan |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUMATRIPTAN
| Product NDC: | 0781-6524 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020626 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080911 |
Package Information of SUMATRIPTAN
| Package NDC: | 0781-6524-86 |
| Package Description: | 6 CONTAINER in 1 BOX (0781-6524-86) > 100 uL in 1 CONTAINER (0781-6524-06) |
NDC Information of SUMATRIPTAN
| NDC Code | 0781-6524-86 |
| Proprietary Name | SUMATRIPTAN |
| Package Description | 6 CONTAINER in 1 BOX (0781-6524-86) > 100 uL in 1 CONTAINER (0781-6524-06) |
| Product NDC | 0781-6524 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sumatriptan |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20080911 |
| Marketing Category Name | NDA |
| Labeler Name | Sandoz Inc |
| Substance Name | SUMATRIPTAN |
| Strength Number | 5 |
| Strength Unit | mg/100uL |
| Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
