FDA NDC Directory · JSON-LD · Markdown

PALSONIFY

NDC 84015-930 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namePALTUSOTINE
Labeler / ManufacturerCrinetics Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA219070
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPALTUSOTINE HYDROCHLORIDE (30 mg/1)
Marketing started20250925
Package count1

External sources

Source: openFDA. Public-domain (CC0).