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Ezetimibe and Simvastatin

NDC 43598-744 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA200909
Dosage form / routeTABLET · ORAL
Active ingredientsEZETIMIBE (10 mg/1)
SIMVASTATIN (20 mg/1)
Marketing started20181120
Marketing ended20271031
Package count3

External sources

Source: openFDA. Public-domain (CC0).