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