# Floxuridine

NDC: 63323-145
Generic name: FLOXURIDINE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRA-ARTERIAL
Marketing started: 20010315

FDA application: ANDA075837

## Active ingredients

- FLOXURIDINE: 500 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8edabc1-67cd-421b-a147-7c1f19f05b8e