# Sodium chloride

NDC: 65219-232
Generic name: SODIUM CHLORIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180723

FDA application: ANDA208122

## Active ingredients

- SODIUM CHLORIDE: 2250 mg/500mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-232"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-232
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=239a5af1-7498-480f-862c-ab7c3d89d183