# CYCLOPHOSPHAMIDE

NDC: 75907-191
Generic name: cyclophosphamide
Labeler / Manufacturer: Dr. Reddy's Labratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240620

FDA application: NDA212501

## Active ingredients

- CYCLOPHOSPHAMIDE ANHYDROUS: 200 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"75907-191"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75907-191
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a5818647-d840-e9d7-c7b8-6541b485e44e