Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD
Lupin Pharmaceuticals recalls 20mg Lisinopril tablets due to potential mix-up with 10mg tablets in sealed bottles. Affected products have NDC 68180-0981-03 and lot # Q000255.
Lower-risk recall
Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling 20mg Lisinopril tablets that may contain 10mg tablets due to a mix-up in sealed bottles. This could lead to incorrect dosing if taken without proper medical supervision. Read more at govinfonow.com/recall/37137-lupin-lisinopril-20mg-tablets-recall-mix-up-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37137-lupin-lisinopril-20mg-tablets-recall-mix-up-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1250-2020
Cite this page
“Lupin Lisinopril 20mg Tablets Recall: Mix-up Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37137-lupin-lisinopril-20mg-tablets-recall-mix-up-risk. Based on FDA recall #D-1250-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1250-2020%22&limit=1).
Why it’s dangerous
The mix-up involves 10mg tablets being mistakenly placed inside sealed bottles labeled as 20mg. If taken without medical supervision, this could cause incorrect dosing. The risk is low because the product is prescription-only and the mix-up is limited to specific bottles.
Who’s affected
People with prescriptions for Lisinopril 20mg tablets who received this specific product. Those with diabetes or kidney issues may be at higher risk due to dosage errors.
How to tell if you have this one
Check for NDC code 68180-0981-03 and lot number Q000255 on the bottle. The product is a 1000-count bottle of 20mg Lisinopril tablets, Rx only, manufactured in Baltimore, MD.
- Brand
Lupin Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Look for NDC 68180-0981-03 and lot number Q000255 on the bottle label.
Questions people ask
Is this product safe to use?
The product may contain 10mg tablets instead of 20mg due to a mix-up. It is prescription-only and should be checked for the correct dosage.
How can I tell if I have the recalled product?
Check for NDC code 68180-0981-03 and lot number Q000255 on the bottle label. The product is a 1000-count bottle of 20mg Lisinopril tablets, Rx only.
What should I do if I have the recalled product?
The recall does not specify a remedy. Check the product details and contact your doctor or pharmacist for guidance.
Contact Lupin Pharmaceuticals
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1250-2020 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-1250-2020 from Lupin Pharmaceuticals. 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-1250-2020 (April 20, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1250-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- 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.