Skip to content
Drug recall · FDA · Published June 12, 2018

Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC

Failed Impurities/Degradation Specifications

🇺🇸 FDA recall #D-0888-2018DrugDr. Reddy's Laboratories, Inc. ›
Take action

Contact the company & request your remedy

Recalling firmDr. Reddy's Laboratories, Inc.107 College Rd E, N/A · 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.
Write-up in progress

We’re still writing up this recall

We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.

Source Page by GovInfoNow · govinfonow.com/recall/40455-dr-reddy-s-laboratories-inc-recalls-atorvastatin-calcium-tablets-40 · Recall date June 12, 2018 · FDA enforcement record: FDA #D-0888-2018

Cite this page

“Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC.” GovInfoNow, recall dated June 12, 2018. https://govinfonow.com/recall/40455-dr-reddy-s-laboratories-inc-recalls-atorvastatin-calcium-tablets-40. Based on FDA recall #D-0888-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0888-2018%22&limit=1).

How to tell if you have this one

  • Brand
    Dr. Reddy's Laboratories, Inc.
  • Category
    Drug
FDA recall event · 3 products

All 3 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 III
  • Status
    Terminated
  • Distribution
    Nationwide in the USA and Puerto Rico
  • NDC
    55111-121-30, 55111-121-60, 55111-121-90, 55111-121-05, 55111-121-10, 55111-122-30, 55111-122-60, 55111-122-90, 55111-122-05, 55111-122-10, 55111-123-30, 55111-123-60, 55111-123-90, 55111-123-05, 55111-123-10
Recall numberProduct, codes & lotsQuantity
D-0886-2018Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-121-90; Lot #: T600327, Exp 07/18; T700213, T700215, Exp 04/1955,126 bottles
D-0887-2018Atorvastatin Calcium Tablets, 20 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-122-90; Lot #: T600328, Exp 07/18; T700214, T700216, Exp 04/1944,894 bottles
D-0888-2018Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC 55111-123-05), Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA; Lot #: a) T600392, T600384, T600353, Exp 08/18; T600427, Exp 09/18; T600435, Exp 10/18; T600492, Exp 11/18; T700006, T700014, T700033, T700035, T700036 12/18; b) T600407, Exp 09/18130,081 bottles
Take action

Contact Dr. Reddy's Laboratories, Inc.

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

Subject: Recall D-0888-2018 — Dr. Reddy's Laboratories, Inc. Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets,

Hello,

I own a Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC that is covered by recall D-0888-2018 from Dr. Reddy's Laboratories, Inc..

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.

Comments are reviewed before they appear. No links, ads, or personal attacks — those get removed.

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-0888-2018 (June 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0888-2018 to see it in context.
  • 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