25% dextrose infant

Generic: 25% dextrose infant

Labeler: hf acquisition co. llc, dba health first
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name 25% dextrose infant
Generic Name 25% dextrose infant
Labeler hf acquisition co. llc, dba health first
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 250 mg/mL

Manufacturer
HF Acquisition Co. LLC, DBA Health First

Identifiers & Regulatory

Product NDC 51662-1213
Product ID 51662-1213_ef6a78fb-553f-a83e-e053-2995a90a6164
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019445
Listing Expiration 2026-12-31
Marketing Start 2018-08-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621213
Hyphenated Format 51662-1213

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 25% dextrose infant (source: ndc)
Generic Name 25% dextrose infant (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 (51662-1213-1) / 10 mL in 1 SYRINGE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

dextrose monohydrate (250 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ef6a78fb-553f-a83e-e053-2995a90a6164", "openfda": {"unii": ["LX22YL083G"], "rxcui": ["727518"], "spl_set_id": ["73d04839-a2bb-65dd-e053-2991aa0a82ca"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA Health First"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, PLASTIC in 1 CARTON (51662-1213-1)  / 10 mL in 1 SYRINGE, PLASTIC", "package_ndc": "51662-1213-1", "marketing_start_date": "20180819"}], "brand_name": "25% Dextrose Infant", "product_id": "51662-1213_ef6a78fb-553f-a83e-e053-2995a90a6164", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1213", "generic_name": "25% Dextrose Infant", "labeler_name": "HF Acquisition Co. LLC, DBA Health First", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "25% Dextrose Infant", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "250 mg/mL"}], "application_number": "NDA019445", "marketing_category": "NDA", "marketing_start_date": "20180819", "listing_expiration_date": "20261231"}