United States · FDA National Drug Code directory
YONSA
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 47335-401_a43dcc9a-83c6-45eb-ab06-20ccc51306bd
- Product NDC
- 47335-401
- Form
- TABLET
- Composition / generic term
- abiraterone acetate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180522
- Source listing expiry
- 20271231
Source-listed ingredients
- ABIRATERONE ACETATE — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE, PLASTIC (47335-401-81) · 47335-401-81
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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