Lupin Pharmaceuticals Inc. recalls Lisinopril and Hydrochlorothiazide Tablets USP, 20 mg/12.5 mg, 500-count bottle, Rx only, Manufactured for: Lupin
Lupin Pharmaceuticals recalls 500-count Lisinopril and Hydrochlorothiazide tablets due to foreign tablets found in product. Consumers should check if they have the specific lot number and contact the company for details.
Lower-risk recall
Presence of Foreign Tablets/Capsules: Product complaint received of one Fenofibrate tablet 145mg observed in 500 s count product bottle.
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling 500-count bottles of Lisinopril and Hydrochlorothiazide tablets because foreign tablets were found in the product. This could pose a risk if the foreign tablets are taken by mistake. Read more at govinfonow.com/recall/38261-lupin-recalls-lisinopril-hydrochlorothiazide-tablets-with-foreign-tablets-found.
Source Summary by GovInfoNow · govinfonow.com/recall/38261-lupin-recalls-lisinopril-hydrochlorothiazide-tablets-with-foreign-tablets-found · Updated October 5, 2026 · FDA enforcement record: FDA #D-1581-2019
Cite this page
“Lupin recalls Lisinopril/Hydrochlorothiazide tablets with foreign tablets found.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38261-lupin-recalls-lisinopril-hydrochlorothiazide-tablets-with-foreign-tablets-found. Based on FDA recall #D-1581-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1581-2019%22&limit=1).
Why it’s dangerous
Foreign tablets were found in the product bottle, which could be taken by mistake. This might lead to unintended medication intake, but the risk is low as the foreign tablets are not the intended medication.
Who’s affected
People who have the 500-count bottle of Lisinopril and Hydrochlorothiazide tablets with lot number H801815 manufactured for Lupin Pharmaceuticals. Those taking the medication as prescribed are most at risk if they accidentally take the foreign tablets.
How to tell if you have this one
Check for the 500-count bottle of Lisinopril and Hydrochlorothiazide tablets with lot number H801815. The product was manufactured for Lupin Pharmaceuticals and sold with NDC 68180-519-02.
- Brand
Lupin- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number H801815 on the bottle to confirm if it is affected.
Questions people ask
Is this product dangerous if taken?
The foreign tablets found in the product are not the intended medication, so taking them by mistake is unlikely to cause harm. However, it is important to check the product details.
How can I tell if I have the recalled product?
Check for the 500-count bottle of Lisinopril and Hydrochlorothiazide tablets with lot number H801815.
What should I do if I have the recalled product?
The recall does not specify a remedy, so contact Lupin Pharmaceuticals for further instructions.
Contact Lupin
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-1581-2019 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-1581-2019 from Lupin. 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-1581-2019 (July 19, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1581-2019 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.