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 25 g/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-6648
Product ID
0409-6648_2f05a8f1-4651-405c-a66b-8e96a46c1db8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019445
Listing Expiration
2027-12-31
Marketing Start
2005-03-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04096648
Hyphenated Format
0409-6648
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
- 25 g/50mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6648-02) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6648-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2f05a8f1-4651-405c-a66b-8e96a46c1db8", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517", "1795514"], "spl_set_id": ["4ed365da-4e62-4329-c1b9-c197ab4fb6e1"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6648-02) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-6648-16)", "package_ndc": "0409-6648-02", "marketing_start_date": "20050331"}], "brand_name": "Dextrose", "product_id": "0409-6648_2f05a8f1-4651-405c-a66b-8e96a46c1db8", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-6648", "generic_name": "DEXTROSE MONOHYDRATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20050331", "listing_expiration_date": "20271231"}