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FDA (Drug enforcement)Recalled 2024-11-18class ii

Viatris Inc: Levothyroxine Sodium Tablets USP, 75 mcg, packaged in a) 90-count bottles (NDC 0378-1805-77) and b) 1000-count bottles (NDC 0378-1805-10), Rx only, Manufactured for: Mylan Pharmaceuticals

Hazard

Superpotent Drug and Subpotent Drug: potency failures obtained

Details from the source

Reason for recall: Superpotent Drug and Subpotent Drug: potency failures obtained Distribution: Nationwide within the United States and Puerto Rico Quantity: 63,077 bottles Lot/code info: Lot #: a) 8177078, Exp. Date May 2025; 8168596, Exp. Date Jan 2025 b) 3199313, Exp. Date May 2025; 3194118, Exp. Date Mar 2025; 3186238, Exp. Date Dec 2024; 3209590, Exp. Date Sep 2025; 3199317, Exp. Date May 2025; 3188733, Exp. Date Jan 2025

Source

Official record: FDA (Drug enforcement)

Republished from the official source above; details can change — the source record controls.

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