FDAAugust 4, 2022drug

Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC 71399-8022-02), Akorn Pharma Manufactured for: Akorn Pharma, Inc., Fairfield, NJ

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.

What to do

FDA enforcement status: Terminated

Brands named

akron pharmaakron

UPCs

7139980220171399802202

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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