Floxuridine
Active substance: floxuridine
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · FLOXURIDINE 500 mg/5mL
United StatesActive
Marketing holder: Fresenius Kabi USA, LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- FLOXURIDINE · 500 mg/5mL
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-3644-7dcc-92ab-1bc8fa81b98b,01a1208f-a424-7a94-9288-c4958cafa5a8,01a12090-3ace-7500-aba7-8ce159aadd5f;count=3 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 63323-145
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRA-ARTERIAL
Sources
- product · openFDA NDC · 63323-145 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 63323-145 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 63323-145 · Verified 2026-10-09 · open in source