FDA NDC Directory · JSON-LD · Markdown

SIMVASTATIN

NDC 72789-316 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078103
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (20 mg/1)
Marketing started20070614
Package count2

External sources

Source: openFDA. Public-domain (CC0).