# Potassium Chloride in Dextrose and Sodium Chloride

NDC: 0990-7904
Generic name: DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
Labeler / Manufacturer: ICU Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200201

FDA application: NDA018362

## Active ingredients

- DEXTROSE MONOHYDRATE: 50 g/1000mL
- POTASSIUM CHLORIDE: 2.98 g/1000mL
- SODIUM CHLORIDE: 4.5 g/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0990-7904"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0990-7904
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8ee14e9-6733-4813-9f21-2b043a5f7188