FDA NDC Directory · JSON-LD · Markdown

Simvastatin

NDC 72189-421 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA078103
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (20 mg/1)
Marketing started20230207
Package count2

External sources

Source: openFDA. Public-domain (CC0).