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FDA NDA 208232: CDER€™s DGE Division's response to OOPD regarding Mycapssa (dated 4/5/24)
FDA NDA 208232: CDER€™s DGE Division's response to OOPD regarding Mycapssa (dated 4/5/24)
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CDER€™s DGE Division response (dated 4/5/24) to the Office of Orphan Drug Products (OOPD)'s consult request regarding Mycapssa (octreotide) (dated July 23, 2020).
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