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Depending on the methods used, a report may record: The reported identity of the submitted substance Measured content Reported purity The analytical method used The testing date The laboratory responsible for the analysis A sample, order or batch identifier Clinical safety or effectiveness Sterility or suitability for human use Nasal absorption or delivery Regulatory approval The composition of another vial, lot or future batch What Is the UK Regulatory Position

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PT-141 (bremelanotide) is the active ingredient in an FDA-approved product for premenopausal hypoactive sexual desire disorder