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In a separate statement, USFDA said AuroMedics Pharma LLC, a unit of Aurobindo Pharma, is recalling 11,520 units of Fondaparinux Sodium Injection in the U.S. market. The medication, an anticoagulant, is used in the treatment of deep vein thrombosis. As per the USFDA, the company is recalling the affected units due to it being “Subpotent Drug: Out of specification for assay”.
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