bicalutamide

NDC 47335-485 · Sun Pharmaceutical Industries, Inc.

Generic namebicalutamide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)BICALUTAMIDE

Strength50 mg/1

Pharmacologic classAndrogen Receptor Antagonists [MoA], Androgen Receptor Inhibitor [EPC]

Marketing categoryANDA

Packages

47335-485-08 — 100 TABLET, FILM COATED in 1 BOTTLE (47335-485-08)

47335-485-18 — 1000 TABLET, FILM COATED in 1 BOTTLE (47335-485-18)

47335-485-83 — 30 TABLET, FILM COATED in 1 BOTTLE (47335-485-83)

47335-485-88 — 100 TABLET, FILM COATED in 1 BOTTLE (47335-485-88)

FDA lists these products with the same active ingredient.

16729-023 — Bicalutamide, 51407-010 — Bicalutamide, 60429-177 — Bicalutamide, 62559-680 — Bicalutamide, 62559-890 — Bicalutamide, 63629-8308 — Bicalutamide, 71205-577 — Bicalutamide, 72578-215 — Bicalutamide, 82804-082 — bicalutamide, 84508-001 — Bicalutamide

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.