United States · FDA National Drug Code directory
Plasma-Lyte 148 (pH 7.4)
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
- 0338-9593_0fe5a11d-9640-4645-8d45-488a04ea6550
- Product NDC
- 0338-9593
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start / end (source format)
- 20241108
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM CHLORIDE — 526 mg/100mL
- SODIUM GLUCONATE — 502 mg/100mL
- SODIUM ACETATE — 368 mg/100mL
- POTASSIUM CHLORIDE — 37 mg/100mL
- MAGNESIUM CHLORIDE — 30 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BAG in 1 CARTON (0338-9593-10) / 1000 mL in 1 BAG (0338-9593-01) · 0338-9593-10
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →