# Ifosfamide

NDC: 63323-142
Generic name: IFOSFAMIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20030128

FDA application: ANDA076078

## Active ingredients

- IFOSFAMIDE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-142"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-142
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a311a947-7b78-4226-bfe0-f4aa0be20e27