Product NDC: | 54868-6052 |
Proprietary Name: | SUMATRIPTAN |
Non Proprietary Name: | sumatriptan |
Active Ingredient(s): | 20 mg/100uL & nbsp; sumatriptan |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6052 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020626 |
Marketing Category: | NDA |
Start Marketing Date: | 20090723 |
Package NDC: | 54868-6052-0 |
Package Description: | 6 CONTAINER in 1 BOX (54868-6052-0) > 100 uL in 1 CONTAINER |
NDC Code | 54868-6052-0 |
Proprietary Name | SUMATRIPTAN |
Package Description | 6 CONTAINER in 1 BOX (54868-6052-0) > 100 uL in 1 CONTAINER |
Product NDC | 54868-6052 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sumatriptan |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20090723 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | SUMATRIPTAN |
Strength Number | 20 |
Strength Unit | mg/100uL |
Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |