infant dextrose

Generic: dextrose

Labeler: henry schein, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name infant dextrose
Generic Name dextrose
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 250 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9844
Product ID 0404-9844_b6d9ad95-3f05-403d-a0c1-a7ff81d9351b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2022-01-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049844
Hyphenated Format 0404-9844

Supplemental Identifiers

RxCUI
727518
UNII
LX22YL083G

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 infant dextrose (source: ndc)
Generic Name dextrose (source: ndc)
Application Number NDA019445 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 250 mg/mL
source: ndc
Packaging
  • 1 SYRINGE in 1 BAG (0404-9844-10) / 10 mL in 1 SYRINGE
source: ndc

Packages (1)

0404-9844-10 1 SYRINGE in 1 BAG (0404-9844-10) / 10 mL in 1 SYRINGE

Ingredients (1)

dextrose monohydrate (250 mg/mL)

Linked Drug Pages (1)

Infant Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "b6d9ad95-3f05-403d-a0c1-a7ff81d9351b", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727518"], "spl_set_id": ["ce71d929-d11e-444c-bd45-e025d5172057"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 BAG (0404-9844-10)  / 10 mL in 1 SYRINGE", "package_ndc": "0404-9844-10", "marketing_start_date": "20220110"}], "brand_name": "Infant Dextrose", "product_id": "0404-9844_b6d9ad95-3f05-403d-a0c1-a7ff81d9351b", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0404-9844", "generic_name": "Dextrose", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Infant Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "250 mg/mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20220110", "listing_expiration_date": "20261231"}