# Potassium Chloride in Dextrose and Sodium Chloride

NDC: 0264-7638
Generic name: DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE
Labeler / Manufacturer: B. Braun Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19880217

FDA application: NDA019630

## Active ingredients

- DEXTROSE, UNSPECIFIED FORM: 5 g/100mL
- POTASSIUM CHLORIDE: .3 g/100mL
- SODIUM CHLORIDE: .45 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0264-7638"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0264-7638
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=59ccc717-c374-41c0-be58-9647df881160