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Alimera Sciences resubmits New Drug Application for ILUVIEN Alimera Sciences, Inc online amoxicillin .S. Food and Medication Administration . At this right time, Alimera awaits the FDA's acceptance of the resubmission and a Prescription Medication User Fee Take action time. Alimera intends to supply that info when it becomes available. Related StoriesTARSA Therapeutics' TBRIA NDA accepted by FDA for reviewMylan announces U.S. Start 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 knowledge with ILUVIEN in European countries.

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