# Sodium Chloride

NDC: 84549-888
Generic name: Sodium Chloride
Labeler / Manufacturer: ProPharma Distribution
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20050228

FDA application: NDA018803

## Active ingredients

- SODIUM CHLORIDE: 9 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84549-888"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84549-888
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48d73434-e65b-dc98-e063-6294a90affa2