# Cyclophosphamide

NDC: 0781-3530
Generic name: Cyclophosphamide
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20240408

FDA application: NDA217150

## Active ingredients

- CYCLOPHOSPHAMIDE: 2000 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3530"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3530
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cf2f4b95-0327-499a-a5a3-51b1bdef68c5