DYMISTA (AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE)
Summary
FDA approved DYMISTA (AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE) by MYLAN SPECIALITY LP. NDA (New Drug) approval (Labeling) on 2024-12-17. SPRAY, METERED, NASAL.
Details
Source
Drug Approval
External ID
NDA202236-21
Action Date
2024-12-17
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
DYMISTA (generic: AZELASTINE HYDROCHLORIDE AND FLUTICASONE PROPIONATE), SPRAY, METERED, NASAL. Application: NDA202236
Company
Context & Analysis
MYLAN SPECIALITY LP has 2 FDA actions in our database.
Frequently Asked Questions
How often does MYLAN SPECIALITY LP have FDA actions?
MYLAN SPECIALITY LP has 2 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA202236-21" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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