Enalapril Maleate Tablets USP — Class III drug recall D-0913-2018
Terminated recall by Wockhardt Limited, reported 2018-07-18, distributed nationwide. Failed Impurities/Degradation Specifications
| Recall number | D-0913-2018 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Recalling firm | Wockhardt Limited, Karodi, India |
| Recall initiated | 2018-06-19 |
| Classified | 2018-07-09 |
| Reported by FDA | 2018-07-18 |
| Terminated | 2020-04-13 |
| Distributed | Nationwide (US) |
| Quantity | 17,628 tablets |
| Reason classes | specification failure |
| NDC | 64679-0923-03 |
| Lot numbers | DR10319, DR10447, DR10996, DS10201 |
Product
Enalapril Maleate Tablets USP; 2.5 mg NDC code 64679-923-03. 1000 Tablets HDPE container pack with Non CRC cap and 2 desiccants further packed in E-flute cartons.
Reason for recall
Failed Impurities/Degradation Specifications
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-0913-2018. 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.