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OLOPATADINE HYDROCHLORIDE

NDC 62332-502 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Generic nameolopatadine hydrochloride
Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209420
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsOLOPATADINE HYDROCHLORIDE (2 mg/mL)
Marketing started20190429
Package count1

External sources

Source: openFDA. Public-domain (CC0).