# Sodium Chloride

NDC: 63323-186
Generic name: SODIUM CHLORIDE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20000810

FDA application: ANDA088912

## Active ingredients

- SODIUM CHLORIDE: 9 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-186"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-186
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f62481fd-fcdb-4be6-ac13-29c590e925c3