FDA NDC Directory · JSON-LD · Markdown

PONVORY

NDC 43068-620 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namePonesimod
Labeler / ManufacturerVanda Pharmaceuticals Inc.
Marketing categoryNew Drug Application (innovator) · App NDA213498
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPONESIMOD (20 mg/1)
Marketing started20210318
Package count1

External sources

Source: openFDA. Public-domain (CC0).