Lupin Limited recalls Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,
Lupin Limited recalls 40mg Pravastatin tablets due to foreign tablets found in one bottle. This is a pharmacy complaint about a Duloxetine capsule being in the product.
Lower-risk recall
Presence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP, 40mg bottle.
Contact the company & request your remedy
What happened, in plain English
Lupin Limited is recalling 40mg Pravastatin Sodium tablets after a pharmacy found Duloxetine Delayed Release Capsules in one bottle. This could lead to incorrect medication use if taken. Read more at govinfonow.com/recall/41048-lupin-pravastatin-tablets-recall-foreign-tablets-found-in-product.
Source Summary by GovInfoNow · govinfonow.com/recall/41048-lupin-pravastatin-tablets-recall-foreign-tablets-found-in-product · Updated October 7, 2026 · FDA enforcement record: FDA #D-0092-2018
Cite this page
“Lupin Pravastatin Tablets Recall: Foreign Tablets Found in Product.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41048-lupin-pravastatin-tablets-recall-foreign-tablets-found-in-product. Based on FDA recall #D-0092-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0092-2018%22&limit=1).
Why it’s dangerous
The product contains foreign tablets (Duloxetine Delayed Release Capsules) that could be taken by mistake. This might cause incorrect medication use if someone takes the foreign tablets instead of the intended Pravastatin.
Who’s affected
People with a prescription for Pravastatin Sodium tablets from Lupin Limited. Those who have the specific bottle with NDC 68180-487-09 and lot # G702459 are most at risk.
How to tell if you have this one
Check for the bottle labeled 'Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only' with NDC 68180-487-09 and lot # G702459. This product was manufactured for Lupin Pharmaceuticals, Inc. in Baltimore, Maryland.
- Brand
Lupin Limited- Category
Drug
What to do — step by step
Check Your Product
Look for the bottle with NDC 68180-487-09 and lot # G702459 to confirm if it's affected.
Questions people ask
Is this product dangerous to take?
The product contains foreign tablets that could be taken by mistake, but the recall is for safety checks, not immediate danger.
How can I tell if I have the recalled product?
Check for the bottle labeled 'Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only' with NDC 68180-487-09 and lot # G702459.
What should I do if I have the recalled product?
The recall doesn't specify a remedy, so check with your pharmacy or healthcare provider for advice.
Contact Lupin Limited
We’ve drafted a message you can send Lupin Limited to request your refund or repair — edit it as you like.
Subject: Recall D-0092-2018 — Lupin Limited Lupin Limited Hello, I own a Lupin Limited that is covered by recall D-0092-2018 from Lupin Limited. 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-0092-2018 (November 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0092-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.