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  5. NDC Package Code: 51662-1413-1 5% Dextrose

NDC Package 51662-1413-1 5% Dextrose

Injection, Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51662-1413-1
Package Description:
50 mL in 1 BAG
Product Code:
51662-1413
Proprietary Name:
5% Dextrose
Non-Proprietary Name:
5% Dextrose
Substance Name:
Dextrose Monohydrate
Usage Information:
Intravenous solutions containing dextrose are indicated for parenteral replenishment of fluid and minimal carbohydrate calories as required by the clinical condition of the patient.
11-Digit NDC Billing Format:
51662141301
NDC to RxNorm Crosswalk:
  • RxCUI: 1795609 - dextrose 5 % in 100 ML Injection
  • RxCUI: 1795609 - 100 ML glucose 50 MG/ML Injection
  • RxCUI: 1795609 - dextrose 5 % per 100 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • DEXTROSE MONOHYDRATE 5 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    NDA016367
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-14-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51662-1413-1?

    The NDC Packaged Code 51662-1413-1 is assigned to a package of 50 ml in 1 bag of 5% Dextrose, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 51662-1413 included in the NDC Directory?

    Yes, 5% Dextrose with product code 51662-1413 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on October 14, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51662-1413-1?

    The 11-digit format is 51662141301. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-151662-1413-15-4-251662-1413-01