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Azelastine Hydrochloride and Fluticasone Propionate

NDC 0480-2157 · HUMAN PRESCRIPTION DRUG · SPRAY, METERED

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208436
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsAZELASTINE HYDROCHLORIDE (137 ug/1)
FLUTICASONE PROPIONATE (50 ug/1)
Marketing started20250908
Package count1

External sources

Source: openFDA. Public-domain (CC0).