# Ceftriaxone Sodium

NDC: 76420-596
Generic name: Ceftriaxone Sodium
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20170630

FDA application: ANDA203702

## 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:"76420-596"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-596
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f01cf0e5-caaf-4759-ba21-50f3aceff523