FDA NDC Directory · JSON-LD · Markdown

Turalio

NDC 65597-407 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namepexidartinib hydrochloride
Labeler / ManufacturerDaiichi Sankyo Inc.
Marketing categoryNew Drug Application (innovator) · App NDA211810
Dosage form / routeCAPSULE · ORAL
Active ingredientsPEXIDARTINIB HYDROCHLORIDE (125 mg/1)
Marketing started20230201
Package count2

External sources

Source: openFDA. Public-domain (CC0).