NDC Code | 17772-132-07 |
Package Description | 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (17772-132-07) |
Product NDC | 17772-132 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Qelbree |
Non-Proprietary Name | Viloxazine Hydrochloride |
Dosage Form | CAPSULE, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20210402 |
Marketing Category Name | NDA |
Application Number | NDA211964 |
Manufacturer | Supernus Pharmaceuticals, Inc |
Substance Name | VILOXAZINE HYDROCHLORIDE |
Strength | 150 |
Strength Unit | mg/1 |
Pharmacy Classes | Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2B6 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Norepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA] |