Actavis’ subsidiary receives FDA complete response letter for progestin-only patch NDA Actavis plc today confirmed that the Firm's subsidiary offers received a complete response letter from the U.S Click to read more about the treatment . Food and Medication Administration because of its New Drug Application for a progestin-only transdermal contraceptive patch for use by ladies to prevent pregnancy.S. Start of generic Fusilev for Injection The Company stated that it intends to function closely with the FDA to address the items raised in the entire response letter which mainly related to questions regarding the difference between the transdermal patch found in the medical trial and the to-be-marketed transdermal patch, which represents a different size/formulation.S., relative to FDA assistance for a contraceptive research..
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