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 70 g/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-0719
Product ID 0338-0719_aa64f648-e931-4a99-9b81-791a3827272c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020047
Listing Expiration 2026-12-31
Marketing Start 1991-07-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03380719
Hyphenated Format 0338-0719

Supplemental Identifiers

RxCUI
237656
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 NDA020047 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 70 g/100mL
source: ndc
Packaging
  • 2000 mL in 1 BAG (0338-0719-06)
source: ndc

Packages (1)

0338-0719-06 2000 mL in 1 BAG (0338-0719-06)

Ingredients (1)

dextrose monohydrate (70 g/100mL)

Linked Drug Pages (1)

DEXTROSE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "aa64f648-e931-4a99-9b81-791a3827272c", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["237656"], "spl_set_id": ["0332f34a-7038-47cc-ba59-d55cad6b73ca"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2000 mL in 1 BAG (0338-0719-06)", "package_ndc": "0338-0719-06", "marketing_start_date": "19910702"}], "brand_name": "DEXTROSE", "product_id": "0338-0719_aa64f648-e931-4a99-9b81-791a3827272c", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0338-0719", "generic_name": "Dextrose monohydrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "70 g/100mL"}], "application_number": "NDA020047", "marketing_category": "NDA", "marketing_start_date": "19910702", "listing_expiration_date": "20261231"}