Abiraterone Acetate

NDC 43598-358 · Dr. Reddys Laboratories Inc

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

43598-358-04 — 120 TABLET in 1 BOTTLE (43598-358-04)

43598-358-31 — 3 BLISTER PACK in 1 CARTON (43598-358-31) / 10 TABLET in 1 BLISTER PACK (43598-358-79)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9597 — Abiraterone acetate, 0378-6920 — abiraterone acetate, 0378-6921 — abiraterone acetate, 0904-6948 — Abiraterone Acetate, 16714-963 — Abiraterone Acetate, 42291-024 — Abiraterone, 42291-073 — ABIRATERONE, 43598-468 — Abiraterone Acetate, 47335-401 — abiraterone acetate, 50268-032 — Abiraterone Acetate, 51407-503 — abiraterone acetate, 51407-989 — abiraterone acetate, 57894-050 — NIRAPARIB TOSYLATE MONOHYDRATE and ABIRATERONE ACETATE, 57894-100 — NIRAPARIB TOSYLATE MONOHYDRATE and ABIRATERONE ACETATE, 57894-150 — abiraterone acetate, 57894-195 — Abiraterone acetate, 60219-1165 — Abiraterone, 60219-1754 — ABIRATERONE, 60505-4327 — Abiraterone Acetate, 60505-4764 — 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.