Apotex Inc. recalls Olanzapine, Orally Disintegrating Tablets, 10 mg, a) 30-count bottle (NDC 60505-3276-03), b) 100-count blister (NDC 605…

Recall date

April 7, 2015

Source

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

Recall number

D-1080-2015

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, 10 mg, a) 30-count bottle (NDC 60505-3276-03), b) 100-count blister (NDC 60505-3276-00), Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada, M9L 1T9