FDA NDC Directory · JSON-LD · Markdown

Sunitinib malate

NDC 16714-676 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213914
Dosage form / routeCAPSULE · ORAL
Active ingredientsSUNITINIB MALATE (12.5 mg/1)
Marketing started20220218
Package count1

External sources

Source: openFDA. Public-domain (CC0).