Sandoz Incorporated recalls Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc.…

Recall date

April 6, 2018

Source

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

Recall number

D-0631-2018

FDA classification

Class III

Brand / firm

Sandoz Incorporated

Sold / distributed

Nationwide in the USA and Puerto Rico

Why it was recalled

Cross Contamination With Other Products: presence of unrelated ingredients (i.e. traces of Lisinopril, Mannitol, Iron, Calcium and Phosphorous).

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

What was recalled

Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.