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Olopatadine hydrochloride

NDC 60505-6221 · HUMAN OTC DRUG · SOLUTION/ DROPS

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA078350
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsOLOPATADINE HYDROCHLORIDE (1 mg/mL)
Marketing started20221006
Package count1

External sources

Source: openFDA. Public-domain (CC0).