Zydus Pharmaceuticals USA Inc recalls Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC
Failed Dissolution Specifications; 9 month long term stability
Recall notice
Failed Dissolution Specifications; 9 month long term stability
Contact the company & request your remedy
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/41812-zydus-pharmaceuticals-usa-inc-recalls-divalproex-sodium-delayed-release-tablets · Recall date March 15, 2017 · FDA enforcement record: FDA #D-0617-2017
Cite this page
“Zydus Pharmaceuticals USA Inc recalls Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC.” GovInfoNow, recall dated March 15, 2017. https://govinfonow.com/recall/41812-zydus-pharmaceuticals-usa-inc-recalls-divalproex-sodium-delayed-release-tablets. Based on FDA recall #D-0617-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0617-2017%22&limit=1).
How to tell if you have this one
- Brand
Zydus Pharmaceuticals (USA) Inc- Category
Drug
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-0617-2017 — Zydus Pharmaceuticals (USA) Inc Zydus Pharmaceuticals USA Inc recalls Divalproex Sodium Delayed Rel Hello, I own a Zydus Pharmaceuticals USA Inc recalls Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC that is covered by recall D-0617-2017 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.
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.
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-0617-2017 (March 15, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0617-2017 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.