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Drug recall · FDA · Published November 26, 2014

Zydus Pharmaceuticals USA Inc recalls Benzonatate Capsules, USP, 200 mg, 100-count bottles, Rx only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad,

Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.

🇺🇸 FDA recall #D-0299-2015DrugZydus Pharmaceuticals (USA) Inc ›
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Recalling firmZydus Pharmaceuticals USA Inc73 Route 31 N, N/A · Pennington, NJ 08534-3601
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/45142-zydus-pharmaceuticals-usa-inc-recalls-benzonatate-capsules-usp-200-mg · Recall date November 26, 2014 · FDA enforcement record: FDA #D-0299-2015

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“Zydus Pharmaceuticals USA Inc recalls Benzonatate Capsules, USP, 200 mg, 100-count bottles, Rx only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad,.” GovInfoNow, recall dated November 26, 2014. https://govinfonow.com/recall/45142-zydus-pharmaceuticals-usa-inc-recalls-benzonatate-capsules-usp-200-mg. Based on FDA recall #D-0299-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0299-2015%22&limit=1).

How to tell if you have this one

  • Brand
    Zydus Pharmaceuticals (USA) Inc
  • Product
    Zydus Pharmaceuticals USA Inc recalls Benzonatate Capsules, USP, 200 mg, 100-count bottles, Rx only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad
  • Category
    Drug
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Contact Zydus Pharmaceuticals (USA) Inc

We’ve drafted a message you can send Zydus Pharmaceuticals (USA) Inc to request your refund or repair — edit it as you like.

Subject: Recall D-0299-2015 — Zydus Pharmaceuticals (USA) Inc Zydus Pharmaceuticals USA Inc recalls Benzonatate Capsules, USP, 20

Hello,

I own a Zydus Pharmaceuticals USA Inc recalls Benzonatate Capsules, USP, 200 mg, 100-count bottles, Rx only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad that is covered by recall D-0299-2015 from Zydus Pharmaceuticals (USA) 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-0299-2015 (November 26, 2014) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0299-2015 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