dextrose

Generic: dextrose monohydrate

Labeler: propharma distribution
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose
Generic Name dextrose monohydrate
Labeler propharma distribution
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 25 g/50mL

Manufacturer
ProPharma Distribution

Identifiers & Regulatory

Product NDC 84549-517
Product ID 84549-517_3a38eb65-2341-a3ef-e063-6294a90ac75d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2005-12-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 84549517
Hyphenated Format 84549-517

Supplemental Identifiers

RxCUI
727517
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
  • 25 g/50mL
source: ndc
Packaging
  • 50 mL in 1 SYRINGE, PLASTIC (84549-517-16)
source: ndc

Packages (1)

84549-517-16 50 mL in 1 SYRINGE, PLASTIC (84549-517-16)

Ingredients (1)

dextrose monohydrate (25 g/50mL)

Linked Drug Pages (1)

Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "3a38eb65-2341-a3ef-e063-6294a90ac75d", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517"], "spl_set_id": ["3842a9c0-8b15-1c94-e063-6394a90ae120"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 SYRINGE, PLASTIC (84549-517-16)", "package_ndc": "84549-517-16", "marketing_start_date": "20250827"}], "brand_name": "Dextrose", "product_id": "84549-517_3a38eb65-2341-a3ef-e063-6294a90ac75d", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "84549-517", "generic_name": "DEXTROSE MONOHYDRATE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20051202", "listing_expiration_date": "20261231"}