Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%)
Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%)
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 Sandoz Incorporated to request your refund or repair — edit it as you like.
Subject: Recall D-0236-2017 — Sandoz Incorporated Sandoz Incorporated recalls Nadolol Tablets, USP, 40mg, packaged in 1000-count Hello, I own a Sandoz Incorporated recalls Nadolol Tablets, USP, 40mg, packaged in 1000-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, that is covered by recall D-0236-2017 from Sandoz Incorporated. 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.
