As we have previously reported on Sandoz’s Biologics License Application (“BLA”) for its proposed biosimilar to Neulasta® (pegfilgrastim), Sandoz received a complete response letter from FDA, and had resubmitted its application after reportedly addressing the issues identified by FDA. Yesterday, the FDA approved Sandoz’s application. The biosimilar, named ZIEXTENZO, is an injectable formulation of pegfilgrastim-bmez, with…
