# Potassium Chloride in Dextrose and Sodium Chloride

NDC: 65219-119
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: 20220831

FDA application: ANDA213445

## Active ingredients

- DEXTROSE MONOHYDRATE: 50 g/1000mL
- POTASSIUM CHLORIDE: 2.98 g/1000mL
- SODIUM CHLORIDE: 9 g/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97001218-086c-430a-9e0d-6c7031c91d94