# Ceftriaxone Sodium

NDC: 0409-7336
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: 20050720
Marketing ended: 20270430
FDA application: ANDA065204

## Active ingredients

- CEFTRIAXONE SODIUM: 2 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-7336"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-7336
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=128bb292-d174-4769-b3e6-9f16617f31e3