# Sodium Chloride

NDC: 84549-049
Generic name: Sodium Chloride
Labeler / Manufacturer: ProPharma Distribution
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 19701209

FDA application: NDA016677

## Active ingredients

- SODIUM CHLORIDE: 9 g/1000mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84549-049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84549-049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3f79fb8b-d0e8-db2a-e063-6394a90ac136