NDC 82249-210 – Capecitabine

Capecitabine 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC82249-210

Product details

Brand name
Capecitabine
Generic name
Capecitabine
Labeler
CivicaScript LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA207652
Marketed since
June 26, 2025
Listing expires
December 31, 2026
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Capecitabine →

Package NDC codes (1)

Package NDCDescriptionSince
82249-210-12120 TABLET, FILM COATED in 1 BOTTLE (82249-210-12)Jun 26, 2025

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