# Ceftriaxone Sodium

NDC: 67184-1007
Generic name: Ceftriaxone Sodium
Labeler / Manufacturer: Qilu Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20160629

FDA application: ANDA203702

## 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:"67184-1007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67184-1007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4cdf0743-c62b-4969-b9c9-4c6400644f6c