FDA NDC Directory · JSON-LD · Markdown

Olopatadine

NDC 70069-017 · HUMAN OTC DRUG · SOLUTION/ DROPS

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206306
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsOLOPATADINE HYDROCHLORIDE (1 mg/mL)
Marketing started20240415
Package count1

External sources

Source: openFDA. Public-domain (CC0).