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: 72603-110_843754c5-046d-4b63-b1d4-344fbb7592fb
Product NDC: 72603-110
Form: TABLET
Composition / generic term: abiraterone acetate
Labeler: NORTHSTAR RX LLC
Marketing category: ANDA
Marketing start / end (source format): 20220307
Source listing expiry: 20271231

Source-listed ingredients

ABIRATERONE ACETATE — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

120 TABLET in 1 BOTTLE (72603-110-01) · 72603-110-01

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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