Lupin Pharmaceuticals recalls 20mg/12.5mg lisinopril and hydrochlorothiazide tablets due to foreign tablets found in sealed bottles. This product is for prescription use only.
Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
Lupin Pharmaceuticals is recalling 100-count bottles of lisinopril and hydrochlorothiazide tablets (20mg/12.5mg) because a sealed bottle was found to contain foreign tablets (atazanavir and ritonavir). This could be dangerous as the foreign tablets are prescription medications that may cause harm if taken.
The recall is for a product mix-up where foreign tablets (atazanavir and ritonavir) were found inside sealed bottles of lisinopril and hydrochlorothiazide. These foreign tablets are prescription medications that could cause harm if taken by mistake.
People who have prescription bottles of lisinopril and hydrochlorothiazide tablets (20mg/12.5mg) from Lupin Pharmaceuticals. Those with the foreign tablets are at higher risk.
Check for 100-count bottles labeled 'Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg' with NDC 68180-519-01 and lot number QA01081. The product is for prescription use only.
Look for the product name, NDC number, and lot number on the bottle to confirm if it's recalled.
The product is not safe to take as it contains foreign tablets that could cause harm.
Check for 100-count bottles labeled 'Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg' with NDC 68180-519-01 and lot number QA01081.
The recall does not specify a remedy, so contact Lupin Pharmaceuticals for guidance.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0532-2025 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0532-2025 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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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.
