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Azelastine Hydrochloride

NDC 47335-779 · HUMAN PRESCRIPTION DRUG · SPRAY, METERED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090423
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsAZELASTINE HYDROCHLORIDE (137 ug/1)
Marketing started20120524
Package count1

External sources

Source: openFDA. Public-domain (CC0).