Class II

Drug Recall: Mycophenolic Acid Delayed-Release Tablets USP, 360 mg, Rx Only, 120 Tablets per bottle, Manufactured by Alkem Laboratories, LTD, INDIA; Distributed by Ascend Laboratories, LLC, Parsippany, NJ 07054, N

Ascend Laboratories, LLC · September 3, 2024

Reason for Recall

Failed Dissolution Specifications

Product Description

Mycophenolic Acid Delayed-Release Tablets USP, 360 mg, Rx Only, 120 Tablets per bottle, Manufactured by Alkem Laboratories, LTD, INDIA; Distributed by Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-427-12.

Distribution

Nationwide in the USA and PR

States Affected

NATIONWIDE

Quantity Affected

117,493 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0668-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.