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Lovastatin

NDC 51655-558 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namelovastatin
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078296
Dosage form / routeTABLET · ORAL
Active ingredientsLOVASTATIN (20 mg/1)
Marketing started20210125
Package count2

External sources

Source: openFDA. Public-domain (CC0).