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
- 68001-524_4bbe764b-4bfd-3862-e063-6394a90a7cc0
- Product NDC
- 68001-524
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Fluorouracil
- Labeler
- BluePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220218
- Source listing expiry
- 20271231
Source-listed ingredients
- FLUOROURACIL — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (68001-524-30) / 10 mL in 1 VIAL (68001-524-28) · 68001-524-30
- 10 VIAL in 1 CARTON (68001-524-31) / 20 mL in 1 VIAL (68001-524-29) · 68001-524-31
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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