Fluorouracil

NDC 51672-4118 · Sun Pharmaceutical Industries, Inc.

Generic nameFluorouracil

Dosage formCREAM

RouteTOPICAL

Active ingredient(s)FLUOROURACIL

Strength50 mg/g

Pharmacologic classNucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]

Marketing categoryANDA

Packages

51672-4118-2 — 1 TUBE in 1 CARTON (51672-4118-2) / 25 g in 1 TUBE

51672-4118-5 — 5 g in 1 TUBE (51672-4118-5)

51672-4118-6 — 1 TUBE in 1 CARTON (51672-4118-6) / 40 g in 1 TUBE

FDA lists these products with the same active ingredient.

16729-276 — Fluorouracil, 16729-542 — Fluorouracil, 21922-041 — Fluorouracil, 21922-049 — Fluorouracil, 25021-215 — fluorouracil, 28105-421 — FLUOROURACIL, 46708-751 — Fluorouracil, 46708-779 — Fluorouracil, 51672-4062 — Fluorouracil, 51672-4063 — Fluorouracil, 51862-362 — FLUOROURACIL, 55150-496 — FLUOROURACIL, 55150-497 — FLUOROURACIL, 55150-498 — FLUOROURACIL, 55150-499 — FLUOROURACIL, 62332-751 — Fluorouracil, 62332-779 — Fluorouracil, 63323-117 — FLUOROURACIL, 68001-524 — Fluorouracil, 68001-525 — Fluorouracil, +20 more

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