# Cefoxitin

NDC: 0143-9877
Generic name: Cefoxitin
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20100312

FDA application: ANDA065238

## Active ingredients

- CEFOXITIN SODIUM: 2 g/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9877"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9877
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d2c449b9-5624-4166-95b1-d7813b3d0445