FDA NDC Directory · JSON-LD · Markdown

Simvastatin

NDC 68084-511 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078103
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (10 mg/1)
Marketing started20110819
Package count1

External sources

Source: openFDA. Public-domain (CC0).