dextrose
Generic: dextrose monohydrate
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
dextrose
Generic Name
dextrose monohydrate
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dextrose monohydrate 250 mg/mL
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 250 mg/mL
Packaging
- 10 CARTON in 1 PACKAGE (0409-1775-10) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC (0409-1775-40)
Packages (1)
Ingredients (1)
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"}