# Potassium Chloride in Dextrose and Sodium Chloride

NDC: 65219-150
Generic name: DEXTROSE MONOHYDRATE, 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: 20220826

FDA application: ANDA213523

## Active ingredients

- DEXTROSE MONOHYDRATE: 25 g/500mL
- POTASSIUM CHLORIDE: .745 g/500mL
- SODIUM CHLORIDE: 2.25 g/500mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-150"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-150
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe5b5182-c859-4c74-b2e0-467be5b2e329