# Ceftriaxone

NDC: 44567-700
Generic name: Ceftriaxone
Labeler / Manufacturer: WG Critical Care, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20080724

FDA application: ANDA065329

## Active ingredients

- CEFTRIAXONE SODIUM: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"44567-700"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=44567-700
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=befd73ff-cb3b-4543-8a8e-bdb9b7fc1ff0