Lupin Pharmaceuticals Inc. recalls Lisinopril and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg, 100 tablet bottle, Rx only, Manufactured by for: Lupin
Lupin Pharmaceuticals recalls 100-tablet bottles of Lisinopril and Hydrochlorothiazide tablets due to brownish/blackish stains and powder inside bottles. Affected products have NDC 68180-518-01 and batch H900575.
Lower-risk recall
Presence of Foreign Substance; Product complaints received related to brownish/blackish stains on the tablets and brownish/blackish powder observed inside the bottles.
Contact the company & request your remedy
What happened, in plain English
Lupin is recalling 100-tablet bottles of Lisinopril and Hydrochlorothiazide tablets that show brownish/blackish stains or powder inside the bottles. This could be a sign of contamination that might affect medication safety. Read more at govinfonow.com/recall/38271-lupin-recalls-lisinopril-hydrochlorothiazide-tablets-with-brown-stains-and-powder.
Source Summary by GovInfoNow · govinfonow.com/recall/38271-lupin-recalls-lisinopril-hydrochlorothiazide-tablets-with-brown-stains-and-powder · Updated October 5, 2026 · FDA enforcement record: FDA #D-1720-2019
Cite this page
“Lupin recalls Lisinopril/Hydrochlorothiazide tablets with brown stains and powder.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38271-lupin-recalls-lisinopril-hydrochlorothiazide-tablets-with-brown-stains-and-powder. Based on FDA recall #D-1720-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1720-2019%22&limit=1).
Why it’s dangerous
The tablets may contain foreign substances that could affect the medication's safety. Brownish/blackish stains or powder inside the bottles indicate possible contamination that might not be safe for use.
Who’s affected
People who have received a 100-tablet bottle of Lisinopril and Hydrochlorothiazide tablets (10 mg/12.5 mg) from Lupin Pharmaceuticals. Those taking these medications are most at risk if the tablets appear stained or contain powder.
How to tell if you have this one
Check for brownish/blackish stains on the tablets or brownish/blackish powder inside the bottle. Products with NDC 68180-518-01 and batch number H900575 are affected.
- Brand
Lupin- Category
Drug
What to do — step by step
Check for Stains or Powder
Inspect the tablets for brownish/blackish stains or powder inside the bottle. If present, stop using the product.
Questions people ask
Why is this product being recalled?
Lupin received complaints about brownish/blackish stains on the tablets and brownish/blackish powder inside the bottles.
What should I do if I have this product?
Check for stains or powder on the tablets or inside the bottle. If present, stop using the product.
Is there a specific batch number I should check?
Yes, affected products have batch number H900575 and NDC 68180-518-01.
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-1720-2019 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-1720-2019 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-1720-2019 (July 17, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1720-2019 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.