FDA NDC Directory · JSON-LD · Markdown

Icosapent Ethyl

NDC 60505-4033 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerApotex Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA209437
Dosage form / routeCAPSULE · ORAL
Active ingredientsICOSAPENT ETHYL (1 g/1)
Marketing started20211216
Marketing ended20270831
Package count1

External sources

Source: openFDA. Public-domain (CC0).