NDC Package 59651-026-55 Amoxicillin And Clavulanate Potassium

Powder, For Suspension Oral - 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:
59651-026-55
Package Description:
150 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Amoxicillin And Clavulanate Potassium
Non-Proprietary Name:
Amoxicillin And Clavulanate Potassium
Substance Name:
Amoxicillin; Clavulanate Potassium
Usage Information:
To reduce the development of drug-resistant bacteria and maintain the effectiveness of amoxicillin and clavulanate potassium for oral suspension and other antibacterial drugs, amoxicillin and clavulanate potassium for oral suspension should be used only to treat infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Amoxicillin and clavulanate potassium for oral suspension is a combination penicillin-class antibacterial and beta-lactamase inhibitor indicated in the treatment of infections due to susceptible isolates of the designated bacteria in the conditions listed below*:
11-Digit NDC Billing Format:
59651002655
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
150 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 617302 - amoxicillin 125 MG / clavulanic acid 31.25 MG in 5 mL Oral Suspension
  • RxCUI: 617302 - amoxicillin 25 MG/ML / clavulanate 6.25 MG/ML Oral Suspension
  • RxCUI: 617302 - amoxicillin (as amoxicillin trihydrate) 25 MG/ML / clavulanate (as clavulanate potassium) 6.25 MG/ML Oral Suspension
  • RxCUI: 617302 - amoxicillin 125 MG / clavulanic acid 31.25 MG per 5 ML Oral Suspension
  • RxCUI: 617322 - amoxicillin 250 MG / clavulanic acid 62.5 MG in 5 mL Oral Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Aurobindo Pharma Limited
    Dosage Form:
    Powder, For Suspension - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a suspension (a liquid preparation containing the solid particles dispersed in the liquid vehicle).
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA209371
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-19-2019
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    59651-026-01100 mL in 1 BOTTLE
    59651-026-7575 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59651-026-55?

    The NDC Packaged Code 59651-026-55 is assigned to a package of 150 ml in 1 bottle of Amoxicillin And Clavulanate Potassium, a human prescription drug labeled by Aurobindo Pharma Limited. The product's dosage form is powder, for suspension and is administered via oral form.

    Is NDC 59651-026 included in the NDC Directory?

    Yes, Amoxicillin And Clavulanate Potassium with product code 59651-026 is active and included in the NDC Directory. The product was first marketed by Aurobindo Pharma Limited on April 19, 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 NDC billing unit for package 59651-026-55?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 150.

    What is the 11-digit format for NDC 59651-026-55?

    The 11-digit format is 59651002655. 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 5-3-2 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
    5-3-259651-026-555-4-259651-0026-55