Home NDC 0338-9593 Plasma-Lyte 148 (pH 7.4)
Product NDC 0338-9593
11-digit product format 003389593
Labeler code 0338
Product ID 0338-9593_0fe5a11d-9640-4645-8d45-488a04ea6550
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Baxter Healthcare Corporation
Marketing category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start 2024-11-08
Substance MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Active strength 30; 37; 368; 526; 502 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Plasma-Lyte 148 (pH 7.4)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 30 mg/100mL SODIUM GLUCONATE 37 mg/100mL SODIUM ACETATE 368 mg/100mL POTASSIUM CHLORIDE 526 mg/100mL MAGNESIUM CHLORIDE 502 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 801109 Internal RxNorm lookup 801357 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0338-9593-01 Plasma-Lyte 148 (pH 7.4) 1000 mL in 1 BAG INJECTION, SOLUTION 1000 2 0338-9593-10 Plasma-Lyte 148 (pH 7.4) 10 in 1 CARTON INJECTION, SOLUTION 10 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0338-9593 PLASMA-LYTE 148 (PH 7.4) (SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] 1 Current NDC, 2 package rows 20241109_fe935c8d-f42d-42e4-8665-0dc66829f231.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 0338-9593-01 00338959301 1000 mL in 1 BAG 1000 ml Historical 0338-9593-10 00338959310 10 BAG in 1 CARTON (0338-9593-10) / 1000 mL in 1 BAG (0338-9593-01) 10 bag 2024-11-08 No No Current