NDC 70518-4483 – Trintellix

Vortioxetine Hydrobromide 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-4483

Product details

Brand name
Trintellix
Generic name
Vortioxetine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA204447
Marketed since
September 24, 2025
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Trintellix →

Package NDC codes (2)

Package NDCDescriptionSince
70518-4483-030 POUCH in 1 BOX (70518-4483-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4483-1)Sep 24, 2025
70518-4483-250 POUCH in 1 BOX (70518-4483-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4483-1)Apr 23, 2026

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