# Potassium Chloride in Dextrose and Sodium Chloride

NDC: 65219-151
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: 20220902

FDA application: ANDA212348

## Active ingredients

- DEXTROSE MONOHYDRATE: 50 g/1000mL
- POTASSIUM CHLORIDE: 1.49 g/1000mL
- SODIUM CHLORIDE: 2.25 g/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0cc6713-4d47-49be-8116-901c99002b6b