FDA recall D-0258-2019

Sandoz Inc · Class II · drug

Product

Isosorbide Dinitrate Tablets, USP 20 mg, 100-count bottles, Rx Only, Distributed by: Sandoz Inc. Princeton, NJ 08540; NDC 0781-1695-01

Reason for recall

Cross Contamination with Other Products

Distribution

Nationwide within the United States

Key facts

Status
Terminated
Initiation date
2018-11-02
Report date
2018-11-21
Termination date
2020-10-02
Voluntary/Mandated
Voluntary: Firm initiated
Location
Princeton, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0258-2019