# Sodium Chloride

NDC: 49230-300
Generic name: Sodium Chloride
Labeler / Manufacturer: Fresenius Medical Care Renal Therapies Group, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20070412

FDA application: ANDA078177

## 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:"49230-300"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49230-300
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af5cdf1a-19f4-11e2-892e-0800200c9a66