# Sodium Chloride

NDC: 63323-530
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: 20200320

FDA application: ANDA209476

## Active ingredients

- SODIUM CHLORIDE: 3 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-530"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-530
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51da05ce-e3c4-4ef5-a845-dc869152e17f