# Ferumoxytol

NDC: 0781-3154
Generic name: ferumoxytol
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20210715

FDA application: ANDA206604

## Active ingredients

- FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE: 510 mg/17mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3154"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3154
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cf94c7fc-13a0-4ac9-bb85-9c38aa704d35