FDA NDC Directory · JSON-LD · Markdown

Icosapent Ethyl

NDC 43598-746 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerDr. Reddy's Laboratories, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209499
Dosage form / routeCAPSULE · ORAL
Active ingredientsICOSAPENT ETHYL (500 mg/1)
Marketing started20230417
Package count1

External sources

Source: openFDA. Public-domain (CC0).