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Drug recall · FDA · Published April 23, 2018

Dr. Reddy's Laboratories, Inc. recalls Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's

Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.

🇺🇸 FDA recall #D-0727-2018DrugDr. Reddy's Laboratories, Inc. ›
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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.
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Source Page by GovInfoNow · govinfonow.com/recall/40606-dr-reddy-s-laboratories-inc-recalls-metoprolol-succinate-extended-release · Recall date April 23, 2018 · FDA enforcement record: FDA #D-0727-2018

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“Dr. Reddy's Laboratories, Inc. recalls Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's.” GovInfoNow, recall dated April 23, 2018. https://govinfonow.com/recall/40606-dr-reddy-s-laboratories-inc-recalls-metoprolol-succinate-extended-release. Based on FDA recall #D-0727-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0727-2018%22&limit=1).

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    Dr. Reddy's Laboratories, Inc.
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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-0727-2018 — Dr. Reddy's Laboratories, Inc. Dr. Reddy's Laboratories, Inc. recalls Metoprolol Succinate Extended

Hello,

I own a Dr. Reddy's Laboratories, Inc. recalls Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's that is covered by recall D-0727-2018 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.

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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-0727-2018 (April 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0727-2018 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