Isosorbide Dinitrate Tablets — Class II drug recall D-0258-2019
Terminated recall by Sandoz Inc, reported 2018-11-21, distributed nationwide. Cross Contamination with Other Products
| Recall number | D-0258-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sandoz Inc, Princeton, NJ, United States |
| Recall initiated | 2018-11-02 |
| Classified | 2018-11-20 |
| Reported by FDA | 2018-11-21 |
| Terminated | 2020-10-02 |
| Distributed | Nationwide (US) |
| Quantity | 18,832 bottles |
| NDC | 00781-1556, 00781-1556-01, 00781-1556-05, 00781-1556-10, 00781-1556-13, 00781-1635, 00781-1635-01, 00781-1635-10, 00781-1635-13, 00781-1695, 00781-1695-01, 00781-1695-10, 00781-1695-13 |
| Expiration dates | 2021-05 |
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0258-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.