Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 40 mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore,
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Recall notice
CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
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Source Page by GovInfoNow · govinfonow.com/recall/43012-lupin-pharmaceuticals-inc-recalls-lisinopril-tablets-usp-40-mg-1000 · Recall date April 6, 2016 · FDA enforcement record: FDA #D-1503-2016
Cite this page
“Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 40 mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore,.” GovInfoNow, recall dated April 6, 2016. https://govinfonow.com/recall/43012-lupin-pharmaceuticals-inc-recalls-lisinopril-tablets-usp-40-mg-1000. Based on FDA recall #D-1503-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1503-2016%22&limit=1).
How to tell if you have this one
- Brand
Lupin Pharmaceuticals Inc.- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
All product distributed domestically in the US. No recalled product was distributed to U.S. Government Agency consignees directly by Lupin. No recalled product was distributed to any foreign consignees by Lupin.- NDC
68180-512-02, 68180-512-30, 68180-512-09, 68180-512-01, 68180-512-03, 68180-513-30, 68180-513-03, 68180-513-01, 68180-513-09, 68180-513-02, 68180-513-05, 68180-517-03, 68180-517-01, 68180-517-30, 68180-517-09, 68180-517-04, 68180-517-02, 68180-980-03, 68180-980-30, 68180-980-01, 68180-980-09, 68180-980-05, 68180-980-02, 68180-981-01, 68180-981-03, 68180-981-30, 68180-981-09, 68180-981-02, 68180-981-05, 68180-982-01, 68180-982-02, 68180-982-30, 68180-982-03, 68180-982-09, 68180-979-01, 68180-979-03, 68180-979-30, 68180-979-09, 68180-514-01, 68180-514-02, 68180-514-03, 68180-514-09, 68180-514-30, 68180-514-05, 68180-515-01, 68180-515-02, 68180-515-03, 68180-515-09, 68180-515-30, 68180-515-05, 68180-516-01, 68180-516-02, 68180-516-03, 68180-516-09, 68180-516-30
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1502-2016 | Lisinopril Tablets USP, 30 mg, packaged in a) 500-count bottles (NDC 68180-516-02) and b) 100-count bottles (NDC 68180-516-01); Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, United States; Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA.; Batch number: H303487, H303488, H303489, Exp 09/16 | 20,556 bottles |
| D-1503-2016 | Lisinopril Tablets USP, 40 mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, United States; Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-517-03.; Batch number: H303449, Exp 09/16 | 5,880 bottles |
Contact Lupin Pharmaceuticals Inc.
We’ve drafted a message you can send Lupin Pharmaceuticals Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1503-2016 — Lupin Pharmaceuticals Inc. Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 40 mg, 1000-c Hello, I own a Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 40 mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, that is covered by recall D-1503-2016 from Lupin Pharmaceuticals Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1503-2016 (April 6, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1503-2016 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.