FDA NDC Directory · JSON-LD · Markdown

SIMVASTATIN

NDC 71335-9642 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA078103
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (20 mg/1)
Marketing started20070614
Package count8

External sources

Source: openFDA. Public-domain (CC0).