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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 217901

ATZUMI (DIHYDROERGOTAMINE MESYLATE)
EQ 5.2MG BASE
Marketing Status: Prescription
Active Ingredient: DIHYDROERGOTAMINE MESYLATE
Proprietary Name: ATZUMI
Dosage Form; Route of Administration: POWDER; NASAL
Strength: EQ 5.2MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N217901
Product Number: 001
Approval Date: Apr 30, 2025
Applicant Holder Full Name: SATSUMA PHARMACEUTICALS INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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