# Floxuridine

NDC: 81643-9270
Generic name: Floxuridine
Labeler / Manufacturer: JND Therapeutics, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRA-ARTERIAL
Marketing started: 20220609

FDA application: ANDA075387

## Active ingredients

- FLOXURIDINE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81643-9270"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81643-9270
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4681f23e-6b5e-433b-b245-3d0b4e64ebb2