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Lovastatin

NDC 70518-2425 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075991
Dosage form / routeTABLET · ORAL
Active ingredientsLOVASTATIN (40 mg/1)
Marketing started20191118
Package count1

External sources

Source: openFDA. Public-domain (CC0).