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
- 43598-468_5e7f1aec-5727-4e71-1a05-55e8eef89e0a
- Product NDC
- 43598-468
- Form
- TABLET
- Composition / generic term
- Abiraterone Acetate
- Labeler
- Dr. Reddys Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230911
- Source listing expiry
- 20261231
Source-listed ingredients
- ABIRATERONE ACETATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 BLISTER PACK in 1 CARTON (43598-468-38) / 10 TABLET in 1 BLISTER PACK (43598-468-79) · 43598-468-38
- 60 TABLET in 1 BOTTLE (43598-468-60) · 43598-468-60
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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