# Cyclophosphamide

NDC: 68001-442
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: 20201019

FDA application: ANDA040745

## Active ingredients

- CYCLOPHOSPHAMIDE: 500 mg/25mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-442"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-442
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7e97b99-83db-42d0-8521-b87fe6467a67