FDA recall D-0259-2019

Product

Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00

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-0259-2019