FDA NDC Directory · JSON-LD · Markdown

Icosapent Ethyl

NDC 0480-0126 · HUMAN PRESCRIPTION DRUG · CAPSULE, LIQUID FILLED

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209525
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsICOSAPENT ETHYL (500 mg/1)
Marketing started20220909
Package count1

External sources

Source: openFDA. Public-domain (CC0).