"35208-009-10" National Drug Code (NDC)

NDC Code	35208-009-10
Package Description	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (35208-009-10)
Product NDC	35208-009
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Desvenlafaxine
Non-Proprietary Name	Desvenlafaxine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20180801
Marketing Category Name	ANDA
Application Number	ANDA204805
Manufacturer	IntelliPharmaCeutics Corp.
Substance Name	DESVENLAFAXINE SUCCINATE
Strength	50
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]