# Ceftriaxone

NDC: 63323-346
Generic name: Ceftriaxone
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20110620

FDA application: ANDA065329

## Active ingredients

- CEFTRIAXONE SODIUM: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-346"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-346
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ea1db43-40fa-417b-8911-ae98092070a0