YONSA
YONSA (abiraterone acetate) tablets
Approved
Approval ID
ec93b41f-88c2-e7ab-e053-2a95a90a636d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 16, 2023
Manufacturers
FDA
Catalent Pharma Solutions, LLC
DUNS: 825745131
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
abiraterone acetate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code11014-0566
Product Classification
G
Generic Name
abiraterone acetate
Product Specifications
Route of AdministrationORAL
Effective DateNovember 16, 2023
FDA Product Classification
INGREDIENTS (1)
ABIRATERONE ACETATEActive
Quantity: 125 mg in 1 1
Code: EM5OCB9YJ6
Classification: ACTIB