Dr Reddy’s Laboratories will benefit from six months of market exclusivity for the first generic rival to Pfizer’s Hemabate carboprost tromethamine single-dose vials that the Indian firm has introduced upon approval in the US.
By securing final approval from the Food and Drug Administration for the 250µg/1ml vials as a competitive generic therapy (CGT), Reddy’s has secured 180-day CGT market exclusivity. “We are pleased to be first-to-market with this product,” commented Marc Kikuchi, who became CEO of the group’s North America generics business earlier this year
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