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Drug recall · FDA · Published July 13, 2022

Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10

Dr. Reddy's recalls 15mg Lansoprazole Delayed-Release tablets due to failed dissolution specifications. This may affect medication effectiveness. Check your product details and contact the manufacturer for instructions.

🇺🇸 FDA recall #D-1287-2022DrugDr. Reddy's ›
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Contact the company & request your remedy

Recalling firmDr. Reddy's Laboratories, Inc.107 College Rd E · Princeton, NJ 08540-6623
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Dr. Reddy's is recalling 15mg Lansoprazole Delayed-Release Orally Disintegrating Tablets because they failed dissolution specifications. This could mean the medication doesn't work properly as intended. Read more at govinfonow.com/recall/34427-dr-reddy-s-lansoprazole-tablets-recall-failed-dissolution-specifications.

Source Summary by GovInfoNow · govinfonow.com/recall/34427-dr-reddy-s-lansoprazole-tablets-recall-failed-dissolution-specifications · Updated September 23, 2026 · FDA enforcement record: FDA #D-1287-2022

Cite this page

“Dr. Reddy's Lansoprazole Tablets Recall: Failed Dissolution Specifications.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/34427-dr-reddy-s-lansoprazole-tablets-recall-failed-dissolution-specifications. Based on FDA recall #D-1287-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1287-2022%22&limit=1).

Why it’s dangerous

The tablets failed to dissolve properly as required by the manufacturer's specifications. This could lead to the medication not working effectively when taken.

Who’s affected

People who have the 15mg Lansoprazole Delayed-Release tablets in blister packs from Dr. Reddy's Laboratories. Those with prescription medication for acid reflux or ulcers are most at risk.

How to tell if you have this one

Check for the blister pack with 100 tablets per carton, 10 packs per box. Look for the NDC code 43598-560-78 and lot number T2100514 on the packaging.

  • Brand
    Dr. Reddy's
  • Product
    Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lotsQuantityNDC
D-1287-2022Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10 Tablets Each, Rx Only, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ 08540, Made in India, blister barcode 4359856079, NDC 43598-560-78; Lot T2100514, Exp 01/20232,892 cartons43598-560-79, 43598-560-78, 43598-561-79, 43598-561-78, 4359856079
D-1288-2022Lansoprazole Delayed-Release Orally Disintegrating Tablets, 35 mg, 100-count blisters per carton, 10 Packs of 10 Tablets Each, Rx Only, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ 08540, Made in India, blister barcode 4359856179, NDC 43598-561-78; Lot T2100515, Exp 01/20232,639 cartons43598-560-79, 43598-560-78, 43598-561-79, 43598-561-78, 4359856179
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify your product has the NDC code 43598-560-78 and lot number T2100514.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall is due to failed dissolution specifications, which may affect medication effectiveness. Dr. Reddy's does not specify if the product is safe to use.

How can I check if my product is recalled?

Check for the NDC code 43598-560-78 and lot number T2100514 on the packaging.

What should I do if I have this product?

The recall record does not specify a remedy, so contact Dr. Reddy's Laboratories for instructions.

Take action

Contact Dr. Reddy's

We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.

Subject: Recall D-1287-2022 — Dr. Reddy's Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters p

Hello,

I own a Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per carton, 10 Packs of 10 that is covered by recall D-1287-2022 from Dr. Reddy's.

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-1287-2022 (July 13, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1287-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on September 23, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA