Pill identification — FDA label match

061 S Pill — Fenofibrate 145 mg (White, Oval)

A white oval tablet with the imprint 061 S matches the FDA label for Fenofibrate 145 mg. Compare every detail below with your pill, and confirm with a pharmacist before relying on it.

Imprint061 S
Imprint parts061 · S (the code is split across the pill — often one part per side)
Generic nameFenofibrate
Active ingredient(s)Fenofibrate 145 mg
Strength145 mg
Dosage formTablet
ColourWhite
ShapeOval
Size18 mm
ScoreNo score
LabelerRemedyrepack Inc.
NDC examples70518-4672-0, 70518-4672-1

What this medicine is

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

Fenofibrate tablets are indicated as adjunctive therapy to diet: to reduce triglyceride (TG) levels in adults with severe hypertriglyceridemia (TG greater than or equal to 500 mg/dL). to reduce elevated low-density lipoprotein cholesterol (LDL-C) in adults with primary hyperlipidemia when use of...
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Frequently asked questions

What pill has the imprint 061 S?

A white oval tablet with the imprint 061 S matches the FDA label for Fenofibrate 145 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 061 S pill look like?

On its FDA label it is described as a white oval tablet, 18 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 061 S · Fenofibrate — all forms & strengths · White pills · Oval pills

Source: FDA label data via DailyMed/openFDA · Label set ID fa9deae7-6cbf-4559-8130-b86b23b6d0ec · Record extracted from the openFDA bulk export of October 29, 2026. Spotted an error? Report it — include the imprint and what looks wrong.