United States · FDA National Drug Code directory
Dextrose and Electrolyte No. 48
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0338-0143_548e1f27-50e8-4b74-b687-3f49bef9d895
- Product NDC
- 0338-0143
- Form
- INJECTION
- Composition / generic term
- Sodium Lactate, Potassium Chloride, Magnesium Chloride, Monobasic Potassium Phosphate, Sodium Chloride and Dextrose monohydrate
- Labeler
- Baxter Healthcare Company
- Marketing category
- NDA
- Marketing start / end (source format)
- 19790202
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 5 g/100mL
- SODIUM LACTATE — 260 mg/100mL
- POTASSIUM CHLORIDE — 141 mg/100mL
- MAGNESIUM CHLORIDE — 31 mg/100mL
- POTASSIUM PHOSPHATE, MONOBASIC — 20 mg/100mL
- SODIUM CHLORIDE — 12 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 500 mL in 1 BAG (0338-0143-03) · 0338-0143-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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