# Potassium Chloride in Dextrose and Sodium Chloride

NDC: 0338-0663
Generic name: Potassium Chloride, Dextrose Monohydrate and Sodium Chloride
Labeler / Manufacturer: Baxter Healthcare Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 19790202

FDA application: NDA018037

## Active ingredients

- DEXTROSE MONOHYDRATE: 5 g/100mL
- POTASSIUM CHLORIDE: 150 mg/100mL
- SODIUM CHLORIDE: 200 mg/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0663"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0663
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c553fed1-3de5-4826-8eff-633b5923bf0b