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
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:59:52
Harmonized routes table
Harmonized routes
INTRAVENOUS

Reported adverse events (FAERS/openFDA)#

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