# Dextrose and Electrolyte No. 48

NDC: 0338-0143
Generic name: Sodium Lactate, Potassium Chloride, Magnesium Chloride, Monobasic Potassium Phosphate, Sodium Chloride and Dextrose monohydrate
Labeler / Manufacturer: Baxter Healthcare Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 19790202

FDA application: NDA017484

## Active ingredients

- DEXTROSE MONOHYDRATE: 5 g/100mL
- MAGNESIUM CHLORIDE: 31 mg/100mL
- POTASSIUM CHLORIDE: 141 mg/100mL
- POTASSIUM PHOSPHATE, MONOBASIC: 20 mg/100mL
- SODIUM CHLORIDE: 12 mg/100mL
- SODIUM LACTATE: 260 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0143"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0143
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b283a454-0c20-4fbf-92d3-dae1f3cd3cad