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
Reported: November 21, 2018 Initiated: November 2, 2018 #D-0260-2019
Product Description
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
Reason for Recall
Cross Contamination with Other Products
Details
- Recalling Firm
- Sandoz Inc
- Units Affected
- 5100 bottles
- Distribution
- Nationwide within the United States
- Location
- Princeton, NJ
Frequently Asked Questions
What product 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. Recalled by Sandoz Inc. Units affected: 5100 bottles.
Why was this product recalled? ▼
Cross Contamination with Other Products
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 21, 2018. Severity: Moderate. Recall number: D-0260-2019.
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