NDC Package 51662-1380-1 Dextrose

Injection Parenteral - View Billable Units, 11-Digit Format, RxNorm

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:
51662-1380-1
Package Description:
1 SYRINGE in 1 CARTON / 50 mL in 1 SYRINGE
Product Code:
Proprietary Name:
Dextrose
Non-Proprietary Name:
Dextrose
Substance Name:
Dextrose Monohydrate
Usage Information:
This product is used to treat low blood sugar levels. Symptoms of low blood sugar include sudden sweating, cold skin, shaking, irritability, fast heartbeat, hunger, blurred vision, dizziness, or tingling hands/feet. It is a good habit to carry glucose tablets, liquid, or gel to treat low blood sugar. If you don't have these reliable forms of glucose, rapidly raise your blood sugar by eating a quick source of sugar such as table sugar, honey, or candy, or drink fruit juice or non-diet soda. To help prevent low blood sugar, eat meals on a regular schedule, and do not skip meals. Check with your doctor or pharmacist about what to do if you miss a meal.
11-Digit NDC Billing Format:
51662138001
NDC to RxNorm Crosswalk:
  • RxCUI: 727517 - dextrose 50 % in 50 ML Prefilled Syringe
  • RxCUI: 727517 - 50 ML glucose 500 MG/ML Prefilled Syringe
  • RxCUI: 727517 - 50 ML dextrose 50 % Prefilled Syringe
  • RxCUI: 727517 - dextrose 25 GM per 50 ML Prefilled Syringe
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hf Acquisition Co Llc, Dba Healthfirst
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Parenteral - Administration by injection, infusion, or implantation.
  • Active Ingredient(s):
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    10-29-2019
    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 51662-1380-1?

    The NDC Packaged Code 51662-1380-1 is assigned to a package of 1 syringe in 1 carton / 50 ml in 1 syringe of Dextrose, a human prescription drug labeled by Hf Acquisition Co Llc, Dba Healthfirst. The product's dosage form is injection and is administered via parenteral form.

    Is NDC 51662-1380 included in the NDC Directory?

    Yes, Dextrose with product code 51662-1380 is active and included in the NDC Directory. The product was first marketed by Hf Acquisition Co Llc, Dba Healthfirst on October 29, 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 51662-1380-1?

    The 11-digit format is 51662138001. 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
    5-4-151662-1380-15-4-251662-1380-01