"47335-804-81" National Drug Code (NDC)

NDC Code	47335-804-81
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-804-81)
Product NDC	47335-804
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Desvenlafaxine
Non-Proprietary Name	Desvenlafaxine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20140130
Marketing Category Name	NDA
Application Number	NDA205583
Manufacturer	Sun Pharma Global FZE
Substance Name	DESVENLAFAXINE FUMARATE MONOHYDRATE
Strength	100
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]