# Cefazolin

NDC: 71205-679
Generic name: Cefazolin
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20170630

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:"71205-679"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-679
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d24529e3-e2b4-46d6-81ba-b7da74501792