FDA NDC Directory · JSON-LD · Markdown

Simvastatin

NDC 65862-050 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077691
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (5 mg/1)
Marketing started20061220
Package count7

External sources

Source: openFDA. Public-domain (CC0).