dextrose monohydrate

Generic: dextrose monohydrate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose monohydrate
Generic Name dextrose monohydrate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 25 g/50mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1453
Product ID 51662-1453_ef7c1a32-f72c-3c5a-e053-2995a90abd43
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2020-01-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621453
Hyphenated Format 51662-1453

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 monohydrate (source: ndc)
Generic Name dextrose monohydrate (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 g/50mL
source: ndc
Packaging
  • 1 SYRINGE in 1 CARTON (51662-1453-1) / 50 mL in 1 SYRINGE
source: ndc

Packages (1)

Ingredients (1)

dextrose monohydrate (25 g/50mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef7c1a32-f72c-3c5a-e053-2995a90abd43", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727517"], "spl_set_id": ["9bd8168d-ab8f-4d70-e053-2995a90ac23c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (51662-1453-1)  / 50 mL in 1 SYRINGE", "package_ndc": "51662-1453-1", "marketing_start_date": "20200111"}], "brand_name": "DEXTROSE MONOHYDRATE", "product_id": "51662-1453_ef7c1a32-f72c-3c5a-e053-2995a90abd43", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1453", "generic_name": "DEXTROSE MONOHYDRATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXTROSE MONOHYDRATE", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "25 g/50mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200111", "listing_expiration_date": "20261231"}