United States · FDA National Drug Code directory
abiraterone acetate
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
- 71921-178_38b4b689-c306-42a0-9df6-5b125314aaab
- Product NDC
- 71921-178
- Form
- TABLET
- Composition / generic term
- abiraterone acetate
- Labeler
- Florida Pharmaceutical Products, LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220815
- Source listing expiry
- 20261231
Source-listed ingredients
- ABIRATERONE ACETATE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE (71921-178-20) · 71921-178-20
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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