dextrose
Generic: dextrose monohydrate
Labeler: medical purchasing solutions, llcDrug Facts
Product Profile
Brand Name
dextrose
Generic Name
dextrose monohydrate
Labeler
medical purchasing solutions, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dextrose monohydrate 250 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71872-7214
Product ID
71872-7214_faceeefa-0646-2e48-e053-6394a90a405f
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
718727214
Hyphenated Format
71872-7214
Supplemental Identifiers
RxCUI
UNII
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
- 1 CARTON in 1 BAG (71872-7214-1) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "faceeefa-0646-2e48-e053-6394a90a405f", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727518"], "spl_set_id": ["ada63d44-3b37-b65d-e053-2a95a90aa088"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 BAG (71872-7214-1) / 1 SYRINGE, PLASTIC in 1 CARTON / 10 mL in 1 SYRINGE, PLASTIC", "package_ndc": "71872-7214-1", "marketing_start_date": "20200605"}], "brand_name": "Dextrose", "product_id": "71872-7214_faceeefa-0646-2e48-e053-6394a90a405f", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "71872-7214", "generic_name": "Dextrose monohydrate", "labeler_name": "Medical Purchasing Solutions, LLC", "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"}