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Azelastine Hydrochloride

NDC 51316-840 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerCVS PHARMACY, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA216421
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsAZELASTINE HYDROCHLORIDE (205.5 ug/1)
Marketing started20250801
Package count5

External sources

Source: openFDA. Public-domain (CC0).