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Simvastatin

NDC 42571-080 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090383
Dosage form / routeTABLET · ORAL
Active ingredientsSIMVASTATIN (80 mg/1)
Marketing started20130613
Package count5

External sources

Source: openFDA. Public-domain (CC0).