dextrose

Generic: dextrose monohydrate

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose
Generic Name dextrose monohydrate
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 100 g/1000mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-0023
Product ID 0338-0023_31bb4a5f-733e-4354-9fbf-138dede4db0f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016694
Listing Expiration 2026-12-31
Marketing Start 1971-01-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03380023
Hyphenated Format 0338-0023

Supplemental Identifiers

RxCUI
1795477 1795480 1795481 1795607 1795609 1795610 1795612 1795616 1795618
UNII
LX22YL083G

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 dextrose (source: ndc)
Generic Name dextrose monohydrate (source: ndc)
Application Number NDA016694 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 g/1000mL
source: ndc
Packaging
  • 250 mL in 1 BAG (0338-0023-02)
  • 500 mL in 1 BAG (0338-0023-03)
  • 1000 mL in 1 BAG (0338-0023-04)
source: ndc

Packages (3)

0338-0023-02 250 mL in 1 BAG (0338-0023-02) 0338-0023-03 500 mL in 1 BAG (0338-0023-03) 0338-0023-04 1000 mL in 1 BAG (0338-0023-04)

Ingredients (1)

dextrose monohydrate (100 g/1000mL)

Linked Drug Pages (1)

DEXTROSE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "31bb4a5f-733e-4354-9fbf-138dede4db0f", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795477", "1795480", "1795481", "1795607", "1795609", "1795610", "1795612", "1795616", "1795618"], "spl_set_id": ["3bb406a9-f5cb-403a-b1bb-5c4facbea3d5"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (0338-0023-02)", "package_ndc": "0338-0023-02", "marketing_start_date": "19710125"}, {"sample": false, "description": "500 mL in 1 BAG (0338-0023-03)", "package_ndc": "0338-0023-03", "marketing_start_date": "19710125"}, {"sample": false, "description": "1000 mL in 1 BAG (0338-0023-04)", "package_ndc": "0338-0023-04", "marketing_start_date": "19710125"}], "brand_name": "DEXTROSE", "product_id": "0338-0023_31bb4a5f-733e-4354-9fbf-138dede4db0f", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0338-0023", "generic_name": "DEXTROSE MONOHYDRATE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "100 g/1000mL"}], "application_number": "NDA016694", "marketing_category": "NDA", "marketing_start_date": "19710125", "listing_expiration_date": "20261231"}