# Fluorouracil

NDC: 46708-779
Generic name: Fluorouracil
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20231018

FDA application: ANDA217676

## Active ingredients

- FLUOROURACIL: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-779"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-779
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b6b0d9e2-c6f0-4523-a33b-b958d32d3a28