NDC Code | 70518-2244-0 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2244-0) |
Product NDC | 70518-2244 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Desvenlafaxine |
Non-Proprietary Name | Desvenlafaxine |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20190801 |
Marketing Category Name | ANDA |
Application Number | ANDA204082 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | DESVENLAFAXINE SUCCINATE |
Strength | 25 |
Strength Unit | mg/1 |
Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA] |