dextrose

Generic: dextrose monohydrate

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose
Generic Name dextrose monohydrate
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 25000 mg/500mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 65219-240
Product ID 65219-240_39549d47-5040-4b1f-8b46-f0dd95832e1e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207449
Listing Expiration 2026-12-31
Marketing Start 2016-10-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65219240
Hyphenated Format 65219-240

Supplemental Identifiers

RxCUI
1795607 1795609 1795610 1795616
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 ANDA207449 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25000 mg/500mL
source: ndc
Packaging
  • 20 BAG in 1 CASE (65219-240-50) / 500 mL in 1 BAG (65219-240-01)
source: ndc

Packages (1)

65219-240-50 20 BAG in 1 CASE (65219-240-50) / 500 mL in 1 BAG (65219-240-01)

Ingredients (1)

dextrose monohydrate (25000 mg/500mL)

Linked Drug Pages (1)

Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "39549d47-5040-4b1f-8b46-f0dd95832e1e", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795607", "1795609", "1795610", "1795616"], "spl_set_id": ["bd250a46-d229-4e80-b5a1-b34169ccecc4"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CASE (65219-240-50)  / 500 mL in 1 BAG (65219-240-01)", "package_ndc": "65219-240-50", "marketing_start_date": "20211110"}], "brand_name": "Dextrose", "product_id": "65219-240_39549d47-5040-4b1f-8b46-f0dd95832e1e", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "65219-240", "generic_name": "Dextrose Monohydrate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25000 mg/500mL"}], "application_number": "ANDA207449", "marketing_category": "ANDA", "marketing_start_date": "20161021", "listing_expiration_date": "20261231"}