FDA NDC Directory · JSON-LD · Markdown

Imbruvica

NDC 57962-014 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameIbrutinib
Labeler / ManufacturerPharmacyclics LLC
Marketing categoryNew Drug Application (innovator) · App NDA210563
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIBRUTINIB (140 mg/1)
Marketing started20180216
Package count1

External sources

Source: openFDA. Public-domain (CC0).