FDA NDC Directory · JSON-LD · Markdown

SUNITINIB MALATE

NDC 43598-047 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA215843
Dosage form / routeCAPSULE · ORAL
Active ingredientsSUNITINIB MALATE (37.5 mg/1)
Marketing started20221130
Package count2

External sources

Source: openFDA. Public-domain (CC0).