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Azelastine Hydrochloride

NDC 71205-449 · HUMAN PRESCRIPTION DRUG · SPRAY, METERED

Generic nameazelastine hydrochloride
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077954
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsAZELASTINE HYDROCHLORIDE (137 ug/1)
Marketing started20100301
Package count1

External sources

Source: openFDA. Public-domain (CC0).