Teva Pharmaceuticals recalled 19,056 bottles of Metoprolol Succinate Extended-Release Tablets, 200 mg, sold nationwide. The recall cites failed dissolution specifications, which could affect how the drug releases in the body. Patients should stop using the product 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 prescription medication distributed nationwide by Teva. The 200 mg strength is formulated for chronic conditions requiring beta‑blocker therapy.
Dissolution failures can alter how quickly or how much active drug is released, potentially compromising blood pressure control.
This recall is not described as part of a broader industry pattern.
Patients with affected bottles may experience reduced drug effectiveness or blood pressure instability. Clinicians should review patients on the affected NDC.
Recall notice lists NDC, lot numbers, and expiration; contact Teva for guidance.
Refunds or replacements follow Teva's process; typically 4-8 weeks after eligibility is confirmed.
Save recall notices, bottle labels, lot numbers, and all correspondence; photograph bottles and labels for records.
- NDC: 45963-678-11\n- Product: Metoprolol Succinate Extended-Release Tablets, 200 mg\n- Bottles per package: 100 tablets\n- Quantity recalled: 19,056 bottles\n- Lot numbers: 0686H251, 0687H251, 10688H251\n- Expiration: 02/2027\n- Brand: METOPROLOL SUCCINATE\n- Manufacturer: Teva Pharmaceuticals USA, Parsippany, NJ\n- Sold nationwide\n- Recall date: 2026-01-29
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