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FDA (Drug enforcement)Recalled 2025-06-20class ii

Lupin Pharmaceuticals Inc.: Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles, Rx only, Mfg for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, Manufactured by: Lupin Lim

Hazard

Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.

Details from the source

Reason for recall: Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg. Distribution: Product was distributed nationwide within the United States. Quantity: 58,968 bottles Lot/code info: Lot #: QA01081, Exp. Date April 2027

Source

Official record: FDA (Drug enforcement)

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

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