FDA NDC Directory · JSON-LD · Markdown

olopatadine hydrochloride

NDC 16571-882 · HUMAN OTC DRUG · SOLUTION

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204392
Dosage form / routeSOLUTION · OPHTHALMIC
Active ingredientsOLOPATADINE HYDROCHLORIDE (1 mg/mL)
Marketing started20250501
Package count1

External sources

Source: openFDA. Public-domain (CC0).