FDA NDC Directory · JSON-LD · Markdown

Icosapent Ethyl

NDC 0054-0621 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209457
Dosage form / routeCAPSULE · ORAL
Active ingredientsICOSAPENT ETHYL (.5 g/1)
Marketing started20201104
Package count1

External sources

Source: openFDA. Public-domain (CC0).