FDA NDC Directory · JSON-LD · Markdown

Sunitinib malate

NDC 63304-094 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213914
Dosage form / routeCAPSULE · ORAL
Active ingredientsSUNITINIB MALATE (50 mg/1)
Marketing started20191225
Package count2

External sources

Source: openFDA. Public-domain (CC0).