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Satsuma Pharmaceuticals Announces U.S. FDA Approval for Atzumi™ (Dihydroergotamine) Nasal Powder for the Acute Treatment of Migraine

Satsuma Pharmaceuticals, Inc., a late-stage biopharmaceutical company dedicated to bringing novel treatments to people who suffer from migraine and other debilitating conditions, and its corporate parent, Shin Nippon Biomedical Laboratories, Ltd. (TSE:2395), today announced that the U.S. Food and Drug Administration (FDA) has approved a 505(b)(2) New Drug Application (NDA) for Atzumi™(dihydroergotamine (DHE)) nasal powder for the acute treatment of migraine with or without aura in adults. Atzumi

articleShin Nippon Biomedical Laboratories, Ltd.April 30, 20258/company/shin-nippon-biomedical-laboratories-ltd/news/satsuma-pharmaceuticals-announces-us-fda-approval-for-atzumitm-dihydroergotamine-nasal-powder-for-the-acute-treatment-of-migraine
Satsuma Pharmaceuticals Announces U.S. FDA Approval for Atzumi™ (Dihydroergotamine) Nasal Powder for the Acute Treatment of Migraine

About this update from Shin Nippon Biomedical Laboratories, Ltd.

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More updates from Shin Nippon Biomedical Laboratories, Ltd.

Shin Nippon Biomedical Laboratories, Ltd.SatsumaDHEacute treatmentSNBLNew Drug Applicationpatientsacute treatment of migrainenasal powder formulationdihydroergotamineFood and Drug Administration