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Azelastine Hydrochloride

NDC 65162-676 · HUMAN PRESCRIPTION DRUG · SPRAY, METERED

Generic nameAzelastine
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204660
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsAZELASTINE HYDROCHLORIDE (1 mg/mL)
Marketing started20170905
Package count1

External sources

Source: openFDA. Public-domain (CC0).