# Cefazolin

NDC: 60505-6244
Generic name: Cefazolin
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220901

FDA application: ANDA209217

## Active ingredients

- CEFAZOLIN SODIUM: 10 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-6244"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-6244
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0e8d4462-7642-4296-a605-6c1493e91ffd