NDC 55154-0256 – Trintellix

Vortioxetine Hydrobromide 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC55154-0256

Product details

Brand name
Trintellix
Generic name
vortioxetine
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA204447
Marketed since
October 2, 2013
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Trintellix →

Package NDC codes (1)

Package NDCDescriptionSince
55154-0256-82520 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-0256-8)Oct 2, 2013

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