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Azelastine Hydrochloride

NDC 47335-938 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078738
Dosage form / routeSOLUTION/ DROPS · INTRAOCULAR
Active ingredientsAZELASTINE HYDROCHLORIDE (.5 mg/mL)
Marketing started20100531
Package count1

External sources

Source: openFDA. Public-domain (CC0).