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Alimera Sciences resubmits New Medication Application for ILUVIEN Alimera Sciences, Inc.S. Food and Medication Administration . At this right time, Alimera awaits the FDA's acceptance of the resubmission and a Prescription Medication User Fee Work date. Alimera intends to provide that info when it becomes available. Related StoriesTARSA Therapeutics' TBRIA NDA recognized by FDA for reviewMylan announces U.S. Release of generic Fusilev for InjectionMylan announces U.S. Launch of generic AXERT tablets In the resubmission, Alimera taken care of immediately questions raised in the FDA's October 2013 complete response letter and provided a safety update, which included commercial encounter with ILUVIEN in European countries.