Belgian value-added medicines firm Hyloris and its development partner AFT Pharmaceuticals have submitted additional data to the US Food and Drug Administration regarding its 505(b)(2) hybrid application for Maxigesic IV (paracetamol/ibuprofen) 1,000mg/300mg. The application was knocked back by the FDA last year when it requested additional information about the dual mode-of-action intravenous pain treatment.
The submission of Hyloris’ “additional extractable & leachable data set” followed a complete response letter received in July 2022 regarding...








