FDA NDC Directory · JSON-LD · Markdown

Sunitinib Malate

NDC 0093-8199 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213803
Dosage form / routeCAPSULE · ORAL
Active ingredientsSUNITINIB MALATE (12.5 mg/1)
Marketing started20211222
Package count1

External sources

Source: openFDA. Public-domain (CC0).