FDA NDC Directory · JSON-LD · Markdown

SULINDAC

NDC 71205-648 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA072711
Dosage form / routeTABLET · ORAL
Active ingredientsSULINDAC (200 mg/1)
Marketing started20100125
Package count3

External sources

Source: openFDA. Public-domain (CC0).