FDA NDC Directory · JSON-LD · Markdown

OLOPATADINE HYDROCHLORIDE

NDC 70069-491 · HUMAN OTC DRUG · SOLUTION/ DROPS

Generic nameOlopatadine Hydrochloride
Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215006
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsOLOPATADINE HYDROCHLORIDE (2 mg/mL)
Marketing started20241220
Package count1

External sources

Source: openFDA. Public-domain (CC0).