# Ceftriaxone Sodium

NDC: 0409-7334
Generic name: Ceftriaxone Sodium
Labeler / Manufacturer: Hospira, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20050517

FDA application: ANDA065168

## Active ingredients

- CEFTRIAXONE SODIUM: 10 g/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-7334"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-7334
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36c07ebf-b091-483e-b2c4-f0fc0c2b4186