dextrose

Generic: dextrose monohydrate

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

Drug Facts

Product Profile

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

dextrose monohydrate 250 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4452
Product ID 70518-4452_3d33f2c3-fdfd-2c0d-e063-6394a90a0bfc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2025-08-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184452
Hyphenated Format 70518-4452

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

Resolved Composition

Strengths
  • 250 mg/mL
source: ndc
Packaging
  • 1 SYRINGE, PLASTIC in 1 CARTON (70518-4452-0) / 10 mL in 1 SYRINGE, PLASTIC (70518-4452-1)
source: ndc

Packages (1)

70518-4452-0 1 SYRINGE, PLASTIC in 1 CARTON (70518-4452-0) / 10 mL in 1 SYRINGE, PLASTIC (70518-4452-1)

Ingredients (1)

dextrose monohydrate (250 mg/mL)

Linked Drug Pages (1)

Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "3d33f2c3-fdfd-2c0d-e063-6394a90a0bfc", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727518"], "spl_set_id": ["e2638b45-1141-4391-971d-c0dea825e41c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, PLASTIC in 1 CARTON (70518-4452-0)  / 10 mL in 1 SYRINGE, PLASTIC (70518-4452-1)", "package_ndc": "70518-4452-0", "marketing_start_date": "20250822"}], "brand_name": "Dextrose", "product_id": "70518-4452_3d33f2c3-fdfd-2c0d-e063-6394a90a0bfc", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "70518-4452", "generic_name": "Dextrose monohydrate", "labeler_name": "REMEDYREPACK INC.", "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": "20250822", "listing_expiration_date": "20261231"}