# CYCLOPHOSPHAMIDE

NDC: 83703-549
Generic name: cyclophosphamide
Labeler / Manufacturer: Bamboo US Bidco LCC
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: 500 mg/25mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83703-549"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83703-549
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2873b99a-830d-0a7b-e063-6394a90a4de7