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abiraterone acetate

NDC 71921-178 · Florida Pharmaceutical Products, LLC.

Generic nameabiraterone acetate
Dosage formTABLET
RouteORAL
Active ingredient(s)ABIRATERONE ACETATE
Strength250 mg/1
Pharmacologic classCytochrome P450 17A1 Inhibitor [EPC], Cytochrome P450 17A1 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA]
Marketing categoryANDA

Packages

71921-178-20 — 120 TABLET in 1 BOTTLE (71921-178-20)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60505-4764 — Abiraterone acetate, 60687-790 — Abiraterone, 64980-418 — Abiraterone acetate, 68001-489 — Abiraterone acetate, 68001-673 — Abiraterone Acetate, 68462-135 — abiraterone acetate, 68462-882 — abiraterone acetate, 69238-1165 — Abiraterone, 69238-1754 — ABIRATERONE, 71921-177 — Abiraterone acetate, 72162-2151 — abiraterone acetate, 72205-030 — Abiraterone acetate, 72205-284 — Abiraterone acetate, 72205-285 — Abiraterone acetate, 72603-110 — abiraterone acetate, 72603-111 — abiraterone acetate, 72789-213 — Abiraterone acetate, 75907-224 — Abiraterone Acetate, 82009-139 — Abiraterone acetate, 82009-140 — Abiraterone acetate, +24 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.