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capecitabine

NDC 72603-303 · NorthStar RxLLC

Generic namecapecitabine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CAPECITABINE
Strength500 mg/1
Pharmacologic classNucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]
Marketing categoryANDA

Packages

72603-303-01 — 120 TABLET, FILM COATED in 1 BOTTLE (72603-303-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62756-239 — Capecitabine, 67877-458 — Capecitabine, 67877-459 — Capecitabine, 68001-487 — CAPECITABINE, 68001-488 — CAPECITABINE, 68001-643 — Capecitabine, 68001-644 — Capecitabine, 69097-948 — Capecitabine, 69097-949 — Capecitabine, 70756-815 — Capecitabine, 70756-816 — Capecitabine, 72205-006 — Capecitabine, 72205-007 — Capecitabine, 72485-204 — Capecitabine, 72485-205 — Capecitabine, 82009-112 — Capecitabine, 82249-207 — Capecitabine, 82249-210 — Capecitabine, 82511-001 — capecitabine, 82511-002 — capecitabine, +15 more

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