Apotex Inc. recalls Olanzapine, Orally Disintegrating Tablets, 5 mg, a) 30-count bottle (NDC 60505-3275-03), b) 100-count blister (NDC 6050…

Recall date

April 7, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-1079-2015

FDA classification

Class III

Brand / firm

Apotex Inc.

Sold / distributed

Nationwide

Why it was recalled

Subpotent drug

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Olanzapine, Orally Disintegrating Tablets, 5 mg, a) 30-count bottle (NDC 60505-3275-03), b) 100-count blister (NDC 60505-3275-00), Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9