Fluorouracil
NDC 51672-4063 · Sun Pharmaceutical Industries, Inc.
Generic nameFluorouracil
Dosage formSOLUTION
RouteTOPICAL
Active ingredient(s)FLUOROURACIL
Strength50 mg/mL
Pharmacologic classNucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]
Marketing categoryANDA
Packages
51672-4063-1 — 1 BOTTLE in 1 CARTON (51672-4063-1) / 10 mL in 1 BOTTLE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
16714-178 — Fluorouracil, 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, 51672-4118 — 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, +20 more