# Potassium Chloride in Sodium Chloride

NDC: 63323-686
Generic name: Sodium Chloride and Potassium Chloride
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210602

FDA application: ANDA212347

## Active ingredients

- POTASSIUM CHLORIDE: 150 mg/100mL
- SODIUM CHLORIDE: 900 mg/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-686"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-686
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2467d57-cd2d-4409-bcc0-50128bd01bba