# Cyclophosphamide

NDC: 0781-3255
Generic name: cyclophosphamide
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS, ORAL
Marketing started: 20141031

FDA application: ANDA204555

## Active ingredients

- CYCLOPHOSPHAMIDE: 2 g/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3255"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3255
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0e9e22fa-178a-42fc-9f82-c303db3b245a