dextrose

Generic: dextrose monohydrate

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

Drug Facts

Product Profile

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

dextrose monohydrate 10 g/100mL

Manufacturer
ICU Medical, Inc.

Identifiers & Regulatory

Product NDC 0990-7938
Product ID 0990-7938_43f81a41-0a45-45f5-840c-768d768edd3b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018080
Listing Expiration 2026-12-31
Marketing Start 2019-11-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09907938
Hyphenated Format 0990-7938

Supplemental Identifiers

RxCUI
1795477
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 NDA018080 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/100mL
source: ndc
Packaging
  • 12 POUCH in 1 CASE (0990-7938-19) / 1 BAG in 1 POUCH / 500 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

dextrose monohydrate (10 g/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "43f81a41-0a45-45f5-840c-768d768edd3b", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["1795477"], "spl_set_id": ["cb578dba-094c-4787-951d-763d12fd06e1"], "manufacturer_name": ["ICU Medical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-7938-19)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7938-19", "marketing_start_date": "20191120"}], "brand_name": "Dextrose", "product_id": "0990-7938_43f81a41-0a45-45f5-840c-768d768edd3b", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "0990-7938", "generic_name": "dextrose monohydrate", "labeler_name": "ICU Medical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "10 g/100mL"}], "application_number": "NDA018080", "marketing_category": "NDA", "marketing_start_date": "20191120", "listing_expiration_date": "20261231"}