FDAFDA · Food and drugs·Recall number D-0261-2019
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
Published November 21, 2018 · Recall initiated: November 2, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Cross Contamination with Other Products
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Sandoz Inc
- Distributor
- Nationwide within the United States
- Lot
- Lot #: JA9534, Exp. 05/2021
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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