FDA NDC Directory · JSON-LD · Markdown

Simvastatin

NDC 69367-375 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211394
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (20 mg/1)
Marketing started20250414
Package count2

External sources

Source: openFDA. Public-domain (CC0).