Global pharma main Lupin received tentative approval from america Food and Drug Administration (USFDA) for its Abbreviated New Drug Application for Selexipag for Injection, 1800 mcg/vial, Single-Dose Vial, to marketplace a everyday equivalent of Uptravi for Injection, 1800 mcg/vial, of Actelion Pharmaceuticals US, Inc. This product may be synthetic at Lupin’s Nagpur facility in India.
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