FDA NDC Directory · JSON-LD · Markdown

ICOSAPENT ETHYL

NDC 16714-636 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameIcosapent ethyl
Labeler / ManufacturerNorthstar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216811
Dosage form / routeCAPSULE · ORAL
Active ingredientsICOSAPENT ETHYL (1 g/1)
Marketing started20250701
Package count1

External sources

Source: openFDA. Public-domain (CC0).