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

Recall Number: D-1353-2022

Firm: Akron Pharma, Inc.

Classification: Class III

Status: Terminated

Report Date: 20220824

Initiation Date: 20220804

Termination Date: 20231204

Reason for Recall

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

Product Description

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