FDA NDC Directory · JSON-LD · Markdown

SULINDAC

NDC 72789-374 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namesulindac
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA072051
Dosage form / routeTABLET · ORAL
Active ingredientsSULINDAC (200 mg/1)
Marketing started20090904
Package count2

External sources

Source: openFDA. Public-domain (CC0).