# Cefoxitin and Dextrose

NDC: 0264-3125
Generic name: CEFOXITIN SODIUM
Labeler / Manufacturer: B. Braun Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20060310

FDA application: NDA065214

## Active ingredients

- CEFOXITIN SODIUM: 2 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0264-3125"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0264-3125
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c7e9485-1ede-411c-8c46-911439332864