# Ceftriaxone

NDC: 0143-9678
Generic name: Ceftriaxone
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20171004

FDA application: ANDA090701

## Active ingredients

- CEFTRIAXONE SODIUM: 10 g/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9678"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9678
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f8776bd-4f5b-427a-849a-6b8338f7997d