Lupin secures tentative USFDA nod for Selexipag for Injection
This product will be manufactured at Lupin's Nagpur facility in India.;
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Mumbai: Global pharma major Lupin Limited today announced that the Company has received tentative approval from the United States Food and Drug Administration (U.S. FDA) for its Abbreviated New Drug Application for Selexipag for Injection, 1800 mcg/vial, Single-Dose Vial, to market a generic equivalent of Uptravi for Injection, 1800 mcg/vial, of Actelion Pharmaceuticals US, Inc.
Selexipag is used for the treatment of pulmonary arterial hypertension to slow down the worsening of symptoms.
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