FDA Drug · D-0877-2026

Paroxetine Extended-Release Tablets, 37.5mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-1318-3

Class II · Ongoing

Failed dissolution specifications.

Affected lots / codes — check yours against thisLot# TY9495, Exp Date: 05/2027.

Recalling firm: Apotex Corp., Weston, FL
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: —
Distribution: US Nationwide.
Recall initiated: September 23, 2026
Classified: September 29, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0877-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

Check this brand across all 8 databases →