FDA NDC Directory · JSON-LD · Markdown

Etodolac

NDC 51655-735 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208834
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsETODOLAC (500 mg/1)
Marketing started20210708
Package count1

External sources

Source: openFDA. Public-domain (CC0).