United States · FDA National Drug Code directory
Plasma-Lyte A
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
- 0338-0221_b7f70780-8da4-45bd-9aa4-78c88a2953d3
- Product NDC
- 0338-0221
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- NDA
- Marketing start / end (source format)
- 19790202
- Source listing expiry
- 20271231
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
- 500 mL in 1 BAG (0338-0221-03) · 0338-0221-03
- 1000 mL in 1 BAG (0338-0221-04) · 0338-0221-04
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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