Teva Pharmaceuticals is recalling 18,780 bottles of Metoprolol Succinate Extended-Release Tablets, 25 mg, distributed nationwide. The recall is due to failed dissolution specifications that could affect dosing. Patients should stop using affected bottles and contact Teva or their healthcare provider for guidance.
Failed Dissolution Specifications
Consumers and healthcare providers should stop using this product immediately. Contact Teva Pharmaceuticals USA, Inc or your healthcare provider for guidance. Notification method: Letter
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Metoprolol succinate extended-release tablets are a generic beta-blocker used to treat high blood pressure, chest pain, and certain heart conditions. They are available in 25 mg extended-release tablets in 100-tablet and 1000-tablet bottles.
Dissolution specification failure means the tablet may not release the drug consistently, potentially leading to underdosing and reduced treatment effectiveness.
This recall is not part of a broader industry pattern.
Patients relying on consistent dosing may experience unmanaged blood pressure or heart rate. There are no reported injuries or deaths in this recall.
Bottle label shows NDC and lot number; official recall page listed in article.
4-6 weeks for recall processing is typical; actual processing times vary by manufacturer and pharmacy.
Keep the recall notice, bottle labels showing NDC and lot numbers, and all correspondence with Teva or your provider.
Product: Metoprolol Succinate Extended-Release Tablets, 25 mg. NDCs: 45963-709-11 (100-tablet bottles) and 45963-709-96 (1000-tablet bottles). Quantity recalled: 18,780 bottles. Manufacturer: Teva Pharmaceuticals USA, Parsippany, NJ 07054. Sold nationwide as Rx-only.
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