"0051-0631-08" National Drug Code (NDC)

NDC Code	0051-0631-08
Package Description	1 BOTTLE in 1 CARTON (0051-0631-08) > 7 TABLET, FILM COATED in 1 BOTTLE
Product NDC	0051-0631
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Vortioxetine
Non-Proprietary Name	Vortioxetine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20131002
End Marketing Date	20200930
Marketing Category Name	APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Application Number	NDA204447
Manufacturer	AbbVie Inc.
Substance Name	VORTIOXETINE HYDROBROMIDE
Strength	10
Strength Unit	mg/1