# SODIUM CHLORIDE

NDC: 0338-9151
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: 450 mg/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-9151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-9151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aeaed9cb-b629-4019-88d2-a916179427de