Skip to content
Drug recall · FDA · Published November 21, 2017

Lupin Pharmaceuticals Inc. recalls Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals,

Failed Dissolution Specification

🇺🇸 FDA recall #D-0097-2018DrugLupin Pharmaceuticals Inc. ›
Take action

Contact the company & request your remedy

Recalling firmLupin Pharmaceuticals Inc.111 S Calvert St Fl 21ST, N/A · Baltimore, MD 21202-6174
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/41043-lupin-pharmaceuticals-inc-recalls-duloxetine-delayed-release-capsules-usp-30 · Recall date November 21, 2017 · FDA enforcement record: FDA #D-0097-2018

Cite this page

“Lupin Pharmaceuticals Inc. recalls Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals,.” GovInfoNow, recall dated November 21, 2017. https://govinfonow.com/recall/41043-lupin-pharmaceuticals-inc-recalls-duloxetine-delayed-release-capsules-usp-30. Based on FDA recall #D-0097-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0097-2018%22&limit=1).

How to tell if you have this one

  • Brand
    Lupin Pharmaceuticals Inc.
  • Product
    Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals
  • Category
    Drug
Take action

Contact Lupin Pharmaceuticals Inc.

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

Subject: Recall D-0097-2018 — Lupin Pharmaceuticals Inc. Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Onl

Hello,

I own a Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals that is covered by recall D-0097-2018 from Lupin Pharmaceuticals 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-0097-2018 (November 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0097-2018 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