The Recall Registry
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Home Prescription medicine Amneal Pharmaceuticals, LLC — Methotrexate…

Food & drug recall · FDAAugust 1, 2024Labelling issue

Amneal Pharmaceuticals, LLC — Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only

Do not stop taking this without speaking to your pharmacist or doctor.

What’s wrong

Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.

The Recall Registry rates this labelling issueFDA Class III: unlikely to cause harm.

What to do

Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.

Who to contact: Recalling firm: Amneal Pharmaceuticals, LLC

The product

Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC# 69238-1423-1

Details

Units affected
12,624 bottles
Recall date
August 1, 2024
Brand
Amneal Pharmaceuticals, LLC
Model, lot or SKU numbers
Lot # BB29124, Exp. 02/28/2026
Where it was distributed

Nationwide in the USA

The official notice

This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.

Their exact wording: Amneal Pharmaceuticals, LLC — Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC# 69238-1423-1

Read it on FDA

Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.

Filed under: Prescription medicine

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