FDA NDC Directory · JSON-LD · Markdown

Simvastatin

NDC 82009-014 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQuallent Pharmaceuticals Health LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200895
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (20 mg/1)
Marketing started20220526
Package count1

External sources

Source: openFDA. Public-domain (CC0).