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Simvastatin

NDC 16714-682 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077691
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSIMVASTATIN (10 mg/1)
Marketing started20061220
Package count3

External sources

Source: openFDA. Public-domain (CC0).