Home NDC 0338-9799 Glucose and Sodium Chloride
Product NDC 0338-9799
11-digit product format 003389799
Labeler code 0338
Product ID 0338-9799_bf7a8e49-ae3a-484a-8437-d8dd72faba49
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Dextrose Anhydrous and Sodium Chloride
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Baxter Healthcare Corporation
Marketing category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start 2024-10-11
Substance DEXTROSE MONOHYDRATE; SODIUM CHLORIDE
Active strength 5.5; .9 g/100mL; g/100mL
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Glucose and Sodium Chloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROSE MONOHYDRATE 5.5 g/100mL SODIUM CHLORIDE .9 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination LX22YL083G Internal UNII lookup 451W47IQ8X Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2698222 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 0338-9799-01 Glucose and Sodium Chloride 1000 mL in 1 BAG INJECTION, SOLUTION 1000 3 0338-9799-12 Glucose and Sodium Chloride 12 in 1 CARTON INJECTION, SOLUTION 12 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0338-9799 GLUCOSE AND SODIUM CHLORIDE (DEXTROSE ANHYDROUS AND SODIUM CHLORIDE) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION] 3 Current NDC, 2 package rows 20250130_1ba918d0-13d0-48bc-8742-658fc0eb47b6.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 0338-9799-01 00338979901 1000 mL in 1 BAG 1000 ml Historical 0338-9799-12 00338979912 12 BAG in 1 CARTON (0338-9799-12) / 1000 mL in 1 BAG (0338-9799-01) 12 bag 2024-10-11 No No Current