FDA NDC Directory · JSON-LD · Markdown

Mulpleta

NDC 59630-551 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameLusutrombopag
Labeler / ManufacturerSHIONOGI INC.
Marketing categoryNew Drug Application (innovator) · App NDA210923
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLUSUTROMBOPAG (3 mg/1)
Marketing started20180827
Package count2

External sources

Source: openFDA. Public-domain (CC0).