United States · FDA National Drug Code directory

Fluorouracil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
46708-779_b6b0d9e2-c6f0-4523-a33b-b958d32d3a28
Product NDC
46708-779
Form
INJECTION, SOLUTION
Composition / generic term
Fluorouracil
Labeler
Alembic Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20231018
Source listing expiry
20261231

Source-listed ingredients

  • FLUOROURACIL — 50 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (46708-779-31) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE · 46708-779-31

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →