Pill identification — FDA label match

5 TL Pill — Vortioxetine 5 mg (Pink, Teardrop)

A pink teardrop tablet with the imprint 5 TL matches the FDA label for Vortioxetine 5 mg. Compare every detail below with your pill, and confirm with a pharmacist before relying on it.

Imprint5 TL
Imprint parts5 · TL (the code is split across the pill — often one part per side)
Brand nameTrintellix
Generic nameVortioxetine
Active ingredient(s)Vortioxetine Hydrobromide 5 mg
Strength5 mg
Dosage formTablet, Film Coated
ColourPink
ShapeTeardrop
Size8 mm
ScoreNo score
LabelerRemedyrepack Inc.
NDC examples70518-4483-0, 70518-4483-1, 70518-4483-2

What this medicine is

According to its FDA-approved label, Vortioxetine is described as follows (reference information only — not advice about whether it is right for anyone):

TRINTELLIX is indicated for the treatment of major depressive disorder (MDD) in adults. TRINTELLIX is indicated for the treatment of major depressive disorder (MDD) in adults ( 1 , 14 ).
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Frequently asked questions

What pill has the imprint 5 TL?

A pink teardrop tablet with the imprint 5 TL matches the FDA label for Vortioxetine 5 mg. Always compare the colour, shape and size as well — short imprints are shared by different medicines — and confirm with a pharmacist.

What does the 5 TL pill look like?

On its FDA label it is described as a pink teardrop tablet, 8 mm, with a score recorded as: no score.

How can I be sure this identification is right?

Check every characteristic — imprint (both sides), colour, shape, size and score — against the pill in your hand. If all of them agree, the pill matches the FDA label shown here, but that is still not a guarantee: counterfeit pills copy real imprints. A pharmacist can confirm the identification in person, and you should never take a pill you are not certain about.

Browse: all pills with imprint 5 TL · Vortioxetine — all forms & strengths · Pink pills · Teardrop pills

Source: FDA label data via DailyMed/openFDA · Label set ID bd0107e5-1cb9-4b40-a6af-fa65fcbe6b4e · Record extracted from the openFDA bulk export of October 29, 2026. Spotted an error? Report it — include the imprint and what looks wrong.