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
- 51672-4118_569a2172-d3a9-45c5-e063-6394a90a3955
- Product NDC
- 51672-4118
- Form
- CREAM
- Composition / generic term
- Fluorouracil
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100305
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOROURACIL — 50 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-4118-2) / 25 g in 1 TUBE · 51672-4118-2
- 5 g in 1 TUBE (51672-4118-5) · 51672-4118-5
- 1 TUBE in 1 CARTON (51672-4118-6) / 40 g in 1 TUBE · 51672-4118-6
Source and coverage
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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.
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