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olopatadine hydrochloride

NDC 45802-104 · HUMAN PRESCRIPTION DRUG · SPRAY

Generic nameOlopatadine Hydrochloride
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA202853
Dosage form / routeSPRAY · NASAL
Active ingredientsOLOPATADINE HYDROCHLORIDE (665 ug/1)
Marketing started20170614
Package count1

External sources

Source: openFDA. Public-domain (CC0).