Superpotent Drug: Failure of assay specifications in the capsule.
Superpotent Drug: Failure of assay specifications in the capsule.
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.
We’ve drafted a message you can send Supernus Pharmaceuticals, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0112-2017 — Supernus Pharmaceuticals, Inc. Supernus Pharmaceuticals, Inc. recalls Trokendi XR (topiramate) exte Hello, I own a Supernus Pharmaceuticals, Inc. recalls Trokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, Manufactured by: Catalent that is covered by recall D-0112-2017 from Supernus 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.
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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.
