dextrose

Generic: dextrose

Labeler: icu medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

dextrose monohydrate 20 g/100mL

Manufacturer
ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-7935
Product ID 0990-7935_6785bd83-c705-41a5-a19c-906f03f380e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018564
Listing Expiration 2026-12-31
Marketing Start 2019-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09907935
Hyphenated Format 0990-7935

Supplemental Identifiers

RxCUI
237649 237650 237656 242694 1795518
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 (source: ndc)
Application Number NDA018564 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 g/100mL
source: ndc
Packaging
  • 12 POUCH in 1 CASE (0990-7935-19) / 1 BAG in 1 POUCH / 500 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

dextrose monohydrate (20 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6785bd83-c705-41a5-a19c-906f03f380e3", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["237649", "237650", "237656", "242694", "1795518"], "spl_set_id": ["b5cb7a5a-bbe8-4217-a82e-da818f7771c9"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-7935-19)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7935-19", "marketing_start_date": "20191001"}], "brand_name": "Dextrose", "product_id": "0990-7935_6785bd83-c705-41a5-a19c-906f03f380e3", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0990-7935", "generic_name": "dextrose", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "20 g/100mL"}], "application_number": "NDA018564", "marketing_category": "NDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}