dextrose

Generic: dextrose monohydrate

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose
Generic Name dextrose monohydrate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 250 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-1775
Product ID 0409-1775_281f40ec-c783-4ef3-875a-48db80a082af
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2006-02-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04091775
Hyphenated Format 0409-1775

Supplemental Identifiers

RxCUI
727518
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 NDA019445 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 250 mg/mL
source: ndc
Packaging
  • 10 CARTON in 1 PACKAGE (0409-1775-10) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1775-40)
source: ndc

Packages (1)

Ingredients (1)

dextrose monohydrate (250 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "281f40ec-c783-4ef3-875a-48db80a082af", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727518"], "spl_set_id": ["672264e3-9709-4bba-2a9d-12bf70c7396a"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (0409-1775-10)  / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1775-40)", "package_ndc": "0409-1775-10", "marketing_start_date": "20060222"}], "brand_name": "Dextrose", "product_id": "0409-1775_281f40ec-c783-4ef3-875a-48db80a082af", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-1775", "generic_name": "Dextrose monohydrate", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "250 mg/mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20060222", "listing_expiration_date": "20261231"}