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
- 68001-525_4bbe6cbf-4510-e811-e063-6294a90a0e28
- Product NDC
- 68001-525
- 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
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (68001-525-27) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE · 68001-525-27
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (68001-525-32) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE · 68001-525-32
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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