FDAFDA · Food and drugs·Recall number D-0236-2017
Nadolol Tablets, USP, 40mg, packaged in 1000-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0781-1182-10
Published January 4, 2017 · Recall initiated: December 22, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%)
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Sandoz Incorporated
- Distributor
- MS and OH.
- Lot
- Lot GG1539
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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