Lisinopril Tablets — Class II drug recall D-1290-2020
Terminated recall by Lupin Pharmaceuticals Inc., reported 2020-06-17, distributed nationwide. Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.
| Recall number | D-1290-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lupin Pharmaceuticals Inc., Baltimore, MD, United States |
| Recall initiated | 2020-05-28 |
| Classified | 2020-06-08 |
| Reported by FDA | 2020-06-17 |
| Terminated | 2021-05-04 |
| Distributed | Nationwide (US) |
| Quantity | 4,224 bottles |
| NDC | 68180-0512, 68180-0512-01, 68180-0512-02, 68180-0512-03, 68180-0512-09, 68180-0512-30, 68180-0513, 68180-0513-01, 68180-0513-02, 68180-0513-03, 68180-0513-05, 68180-0513-09, 68180-0513-30, 68180-0514, 68180-0514-01, 68180-0514-02, 68180-0514-03, 68180-0514-05, 68180-0514-09, 68180-0514-30, 68180-0515, 68180-0515-01, 68180-0515-02, 68180-0515-03, 68180-0515-05 and 40 more |
| Lot numbers | Q900683 |
| Expiration dates | 2022-10-31 |
Product
Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Nagpur - 441 108, India, NDC 68180-513-03.
Reason for recall
Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.
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-1290-2020. 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.