FDA NDC Directory · JSON-LD · Markdown

SULINDAC

NDC 24658-770 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPuraCap Laboratories LLC dba Blu Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA072710
Dosage form / routeTABLET · ORAL
Active ingredientsSULINDAC (150 mg/1)
Marketing started20161114
Package count2

External sources

Source: openFDA. Public-domain (CC0).