# Sodium Chloride

NDC: 0409-6660
Generic name: SODIUM CHLORIDE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20050729

FDA application: NDA018897

## Active ingredients

- SODIUM CHLORIDE: 5.84 g/40mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-6660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-6660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=018a8807-1331-41c3-4889-c7ec502a9043