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The patient presented classical features of ochronotic effects comprising scleral melanosis, arthropathy, and constrictive lung functions

NDA submission: Q3 2027 Approval: Mid-2028 Launch: Late 2028 or early 2029 After NDA Submission: The FDA Review Process Month 02: Filing Decision (60 Days) The FDA reviews the application for completeness

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Healthcare providers should consider several factors when making this decision

[DOI] [PubMed] [Google Scholar] 100.Rosenstock J, Fras JP, Rodbard HW, et al

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