# SODIUM CHLORIDE

NDC: 0338-9662
Generic name: sodium chloride
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19921207

FDA application: NDA020178

## Active ingredients

- SODIUM CHLORIDE: 900 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-9662"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-9662
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9e72418a-376e-4637-99ad-d13c904a7986