FDA Drug Recalls

Recalls / Generics / Paroxetine

Paroxetine

4 FDA drug recalls involving generic “Paroxetine.

DateClassProductFirm
2017-11-20Class IIParoxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-099-05), and c) 1000 Zydus Pharmaceuticals USA Inc
2017-10-24Class IIParoxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, ColAmerisource Health Services
2017-08-18Class IIParoxetine tablets USP, 30mg, 30-count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, InZydus Pharmaceuticals USA Inc
2017-06-22Class IIIParoxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin PharmaceutLupin Pharmaceuticals Inc.