# Ceftriaxone

NDC: 0338-5002
Generic name: Ceftriaxone Sodium
Labeler / Manufacturer: Baxter Healthcare Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20050823

FDA application: ANDA065224

## Active ingredients

- CEFTRIAXONE SODIUM: 1 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-5002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-5002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c5c2d3f-5038-41a1-a2fe-4dcd048dbac1