FDA NDC Directory · JSON-LD · Markdown

Simvastatin

NDC 72865-308 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerXLCare Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200895
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (40 mg/1)
Marketing started20260121
Package count5

External sources

Source: openFDA. Public-domain (CC0).