Product NDC: | 43376-106 |
Proprietary Name: | Sumavel DosePro |
Non Proprietary Name: | sumatriptan |
Active Ingredient(s): | 6 mg/.5mL & nbsp; sumatriptan |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43376-106 |
Labeler Name: | Zogenix, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022239 |
Marketing Category: | NDA |
Start Marketing Date: | 20090715 |
Package NDC: | 43376-106-51 |
Package Description: | 1 SYRINGE, GLASS in 1 CARTON (43376-106-51) > .5 mL in 1 SYRINGE, GLASS |
NDC Code | 43376-106-51 |
Proprietary Name | Sumavel DosePro |
Package Description | 1 SYRINGE, GLASS in 1 CARTON (43376-106-51) > .5 mL in 1 SYRINGE, GLASS |
Product NDC | 43376-106 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sumatriptan |
Dosage Form Name | INJECTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 20090715 |
Marketing Category Name | NDA |
Labeler Name | Zogenix, Inc. |
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] |