# CYCLOPHOSPHAMIDE

NDC: 10019-944
Generic name: cyclophosphamide
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS, ORAL
Marketing started: 20080521

FDA application: ANDA040745

## Active ingredients

- CYCLOPHOSPHAMIDE: 1 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10019-944"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10019-944
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cef038cc-efab-46d9-99c2-95bb11d6c9bc