# Sodium Chloride

NDC: 0487-4301
Generic name: Sodium Chloride
Labeler / Manufacturer: Nephron Pharmaceuticals Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20200604

FDA application: ANDA211968

## Active ingredients

- SODIUM CHLORIDE: 9 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0487-4301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0487-4301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a4edf2d5-a9ff-30d4-e053-2995a90a5650