# Cefuroxime

NDC: 0143-9568
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: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20040109

FDA application: ANDA065048

## Active ingredients

- CEFUROXIME SODIUM: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9568"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9568
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19902965-d2d6-433f-982d-0095014df4e8