Plasma-Lyte 148 (pH 7.4)

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Plasma-Lyte 148 (pH 7.4)
Generic name
SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE
Manufacturer
Baxter Healthcare Corporation
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
fe935c8d-f42d-42e4-8665-0dc66829f231
SPL ID
0fe5a11d-9640-4645-8d45-488a04ea6550
Version
2
Effective date
2024-11-08
Source export date
2026-10-30
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:00:08
Harmonized routes table
Harmonized routes
INTRAVENOUS

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.