US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 2, 2018 (8 years ago)

Isosorbide Dinitrate Tablets, USP 20 mg,100-count bottles, Rx Only Manufactured by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Cross Contamination with Other Products

What was recalled

Isosorbide Dinitrate Tablets, USP 20 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-222-00

Recalling firm
Sandoz Inc
NDC code
68001-222-00
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0261-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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