Isosorbide Dinitrate Tablets — Class II drug recall D-0261-2019
Terminated recall by Sandoz Inc, reported 2018-11-21, distributed nationwide. Cross Contamination with Other Products
| Recall number | D-0261-2019 |
|---|---|
| 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 | 1,550 bottles |
| NDC | 68001-0222-00 |
| Lot numbers | JA9534 |
| Expiration dates | 2021-05 |
Product
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
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-0261-2019. 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.