glucose and sodium chloride

Generic: dextrose anhydrous and sodium chloride

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE Inactive Finished

Drug Facts

Product Profile

Brand Name glucose and sodium chloride
Generic Name dextrose anhydrous and sodium chloride
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 5.5 g/100mL, sodium chloride .9 g/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-9799
Product ID 0338-9799_bf7a8e49-ae3a-484a-8437-d8dd72faba49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Listing Expiration 2026-12-31
Marketing Start 2024-10-11

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03389799
Hyphenated Format 0338-9799

Supplemental Identifiers

RxCUI
2698222
UNII
LX22YL083G 451W47IQ8X

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name glucose and sodium chloride (source: ndc)
Generic Name dextrose anhydrous and sodium chloride (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5.5 g/100mL
  • .9 g/100mL
source: ndc
Packaging
  • 12 BAG in 1 CARTON (0338-9799-12) / 1000 mL in 1 BAG (0338-9799-01)
source: ndc

Packages (1)

0338-9799-12 12 BAG in 1 CARTON (0338-9799-12) / 1000 mL in 1 BAG (0338-9799-01)

Ingredients (2)

dextrose monohydrate (5.5 g/100mL) sodium chloride (.9 g/100mL)

Linked Drug Pages (1)

Glucose and Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "bf7a8e49-ae3a-484a-8437-d8dd72faba49", "openfda": {"unii": ["LX22YL083G", "451W47IQ8X"], "rxcui": ["2698222"], "spl_set_id": ["1ba918d0-13d0-48bc-8742-658fc0eb47b6"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BAG in 1 CARTON (0338-9799-12)  / 1000 mL in 1 BAG (0338-9799-01)", "package_ndc": "0338-9799-12", "marketing_start_date": "20241011"}], "brand_name": "Glucose and Sodium Chloride", "product_id": "0338-9799_bf7a8e49-ae3a-484a-8437-d8dd72faba49", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0338-9799", "generic_name": "Dextrose Anhydrous and Sodium Chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glucose and Sodium Chloride", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5.5 g/100mL"}, {"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_start_date": "20241011", "listing_expiration_date": "20261231"}