# Cefazolin

NDC: 63323-238
Generic name: Cefazolin Sodium
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20110614

FDA application: ANDA065306

## 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:"63323-238"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-238
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47a8928f-708d-418a-829b-36eded96bac0