yonsa
Generic: abiraterone acetate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
yonsa
Generic Name
abiraterone acetate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
TABLET
Routes
Active Ingredients
abiraterone acetate 125 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
47335-401
Product ID
47335-401_aea1d51d-d946-4029-a05e-88dbd32c1e9d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA210308
Listing Expiration
2026-12-31
Marketing Start
2018-05-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47335401
Hyphenated Format
47335-401
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
yonsa (source: ndc)
Generic Name
abiraterone acetate (source: ndc)
Application Number
NDA210308 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/1
Packaging
- 120 TABLET in 1 BOTTLE, PLASTIC (47335-401-81)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aea1d51d-d946-4029-a05e-88dbd32c1e9d", "openfda": {"unii": ["EM5OCB9YJ6"], "rxcui": ["2046579", "2046585"], "spl_set_id": ["b8967e10-f768-47ce-ac9e-2324c8390132"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (47335-401-81)", "package_ndc": "47335-401-81", "marketing_start_date": "20180522"}], "brand_name": "YONSA", "product_id": "47335-401_aea1d51d-d946-4029-a05e-88dbd32c1e9d", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 17A1 Inhibitor [EPC]", "Cytochrome P450 17A1 Inhibitors [MoA]", "Cytochrome P450 2C8 Inhibitors [MoA]", "Cytochrome P450 2D6 Inhibitors [MoA]"], "product_ndc": "47335-401", "generic_name": "abiraterone acetate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "YONSA", "active_ingredients": [{"name": "ABIRATERONE ACETATE", "strength": "125 mg/1"}], "application_number": "NDA210308", "marketing_category": "NDA", "marketing_start_date": "20180522", "listing_expiration_date": "20261231"}