# SODIUM CHLORIDE

NDC: 0409-1141
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: 20050430

FDA application: NDA018897

## Active ingredients

- SODIUM CHLORIDE: 234 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-1141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-1141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af6aebad-ef03-4d19-9a40-18e5a278b812