NDC Package 0264-7625-00 Potassium Chloride In Dextrose

Dextrose And Potassium Chloride Solution Intravenous - 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:
0264-7625-00
Package Description:
12 CONTAINER in 1 CASE / 1000 mL in 1 CONTAINER
Product Code:
Proprietary Name:
Potassium Chloride In Dextrose
Non-Proprietary Name:
Dextrose And Potassium Chloride
Substance Name:
Dextrose; Potassium Chloride
Usage Information:
This intravenous solutionĀ is indicated for use in adults and pediatric patients as a sourceĀ of electrolytes, calories, and water for hydration.
11-Digit NDC Billing Format:
00264762500
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 309783 - potassium chloride 20 MEQ / glucose 5 % in 1000 ML Injection
  • RxCUI: 309783 - 1000 ML glucose 50 MG/ML / potassium chloride 0.02 MEQ/ML Injection
  • RxCUI: 309783 - 1000 ML Glucose 50 MG/ML / K+ Chloride 0.02 MEQ/ML Injection
  • RxCUI: 309783 - 1000 ML Glucose 50 MG/ML / Pot Chloride 0.02 MEQ/ML Injection
  • RxCUI: 309783 - dextrose 5 % / potassium chloride 20 MEQ per 1000 ML Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    B. Braun Medical Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Sample Package:
    No
    FDA Application Number:
    NDA019699
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    09-29-1989
    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 0264-7625-00?

    The NDC Packaged Code 0264-7625-00 is assigned to a package of 12 container in 1 case / 1000 ml in 1 container of Potassium Chloride In Dextrose, a human prescription drug labeled by B. Braun Medical Inc.. The product's dosage form is solution and is administered via intravenous form.

    Is NDC 0264-7625 included in the NDC Directory?

    Yes, Potassium Chloride In Dextrose with product code 0264-7625 is active and included in the NDC Directory. The product was first marketed by B. Braun Medical Inc. on September 29, 1989 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 NDC billing unit for package 0264-7625-00?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0264-7625-00?

    The 11-digit format is 00264762500. 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 4-4-2 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
    4-4-20264-7625-005-4-200264-7625-00