# Cefazolin

NDC: 60505-6243
Generic name: Cefazolin
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20220901

FDA application: ANDA203661

## Active ingredients

- CEFAZOLIN SODIUM: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-6243"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-6243
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=37a626aa-96dc-4c4d-bfbc-be4f328f918b