Brintellix

Product NDC

64764-580

11-digit product format

647640580

Labeler code

64764

Product ID

64764-580_cc70d6dd-e54b-483d-83f5-762a6cce455a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

vortioxetine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Takeda Pharmaceuticals America, Inc.

Application

NDA204447

Marketing category

NDA

Marketing start

2013-10-02

Marketing end

0000-00-00

Substance

VORTIOXETINE HYDROBROMIDE

Active strength

20 mg/1

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record