NDC 82804-082 – Bicalutamide

Bicalutamide 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82804-082

Product details

Brand name
Bicalutamide
Generic name
Bicalutamide
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA079110
Marketed since
December 15, 2014
Listing expires
December 31, 2026
Pharmacologic class
Androgen Receptor Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Bicalutamide →

Package NDC codes (1)

Package NDCDescriptionSince
82804-082-9090 TABLET, FILM COATED in 1 BOTTLE (82804-082-90)Mar 13, 2024

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