Sandoz Inc recalls Isosorbide Dinitrate Tablets, USP 10 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 Fo…

Recall date

November 2, 2018

Source

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

Recall number

D-0260-2019

FDA classification

Class II

Brand / firm

Sandoz Inc

Sold / distributed

Nationwide within the United States

Why it was recalled

Cross Contamination with Other Products

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Isosorbide Dinitrate Tablets, USP 10 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-225-00