Skip to content
Drug recall · FDA · Published June 27, 2016

Sun Pharmaceutical Industries, Inc. recalls buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Only 60 tablets Distributed by Sun Pharmaceutical

Failed Dissolution Specifications

🇺🇸 FDA recall #D-1446-2016DrugSUN PHARMACEUTICAL INDUSTRIES INC ›
Take action

Contact the company & request your remedy

Recalling firmSun Pharmaceutical Industries, Inc.270 Prospect Plains Rd, N/A · Cranbury, NJ 08512-3605
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/42572-sun-pharmaceutical-industries-inc-recalls-bupropion-hydrochloride-extended-release-tablets · Recall date June 27, 2016 · FDA enforcement record: FDA #D-1446-2016

Cite this page

“Sun Pharmaceutical Industries, Inc. recalls buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Only 60 tablets Distributed by Sun Pharmaceutical.” GovInfoNow, recall dated June 27, 2016. https://govinfonow.com/recall/42572-sun-pharmaceutical-industries-inc-recalls-bupropion-hydrochloride-extended-release-tablets. Based on FDA recall #D-1446-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1446-2016%22&limit=1).

How to tell if you have this one

  • Brand
    SUN PHARMACEUTICAL INDUSTRIES INC
  • Category
    Drug
Take action

Contact SUN PHARMACEUTICAL INDUSTRIES INC

We’ve drafted a message you can send SUN PHARMACEUTICAL INDUSTRIES INC to request your refund or repair — edit it as you like.

Subject: Recall D-1446-2016 — SUN PHARMACEUTICAL INDUSTRIES INC Sun Pharmaceutical Industries, Inc. recalls buPROPion Hydrochlori

Hello,

I own a Sun Pharmaceutical Industries, Inc. recalls buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Only 60 tablets Distributed by Sun Pharmaceutical that is covered by recall D-1446-2016 from SUN PHARMACEUTICAL INDUSTRIES 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-1446-2016 (June 27, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1446-2016 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