# Cyclophosphamide

NDC: 68001-695
Generic name: cyclophosphamide
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS, ORAL
Marketing started: 20260315

FDA application: ANDA218644

## Active ingredients

- CYCLOPHOSPHAMIDE: 1 g/50mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-695"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-695
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d3396d8-4c03-4a28-890a-d87c6c53a74e