# Cefuroxime

NDC: 0143-9569
Generic name: Cefuroxime
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: 20040109

FDA application: ANDA065046

## Active ingredients

- CEFUROXIME SODIUM: 7.5 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9569"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9569
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=79f5cf6f-a5e2-49a2-9704-fa1bd21338c3