FDA NDC Directory · JSON-LD · Markdown

SIMVASTATIN

NDC 68180-465 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078103
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (80 mg/1)
Marketing started20160105
Package count3

External sources

Source: openFDA. Public-domain (CC0).