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  5. NDC Package Code: 59088-727-00 Clofenax

NDC Package 59088-727-00 Clofenax

Diclofenac Sodium,Kinesiology Tape Kit - 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:
59088-727-00
Package Description:
1 KIT in 1 KIT * 1 BOTTLE, DROPPER in 1 CARTON (51672-1358-2) / 150 mL in 1 BOTTLE, DROPPER
Product Code:
59088-727
Proprietary Name:
Clofenax
Non-Proprietary Name:
Diclofenac Sodium, Kinesiology Tape
Usage Information:
Diclofenac sodium topical solution, USP is indicated for the treatment of signs and symptoms of osteoarthritis of the knee(s) (1).
11-Digit NDC Billing Format:
59088072700
NDC to RxNorm Crosswalk:
  • RxCUI: 857700 - diclofenac sodium 1.5 % Topical Solution
  • RxCUI: 857700 - diclofenac sodium 15 MG/ML Topical Solution
  • RxCUI: 857700 - diclofenac sodium 1.5 % (as diclofenac sodium 16.05 MG/ML) Topical Solution
  • RxCUI: 857700 - diclofenac sodium 16.05 MG per 1 ML Topical Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Puretek Corporation
    Dosage Form:
    Kit - A packaged collection of related material.
    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:
    12-09-2020
    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 59088-727-00?

    The NDC Packaged Code 59088-727-00 is assigned to a package of 1 kit in 1 kit * 1 bottle, dropper in 1 carton (51672-1358-2) / 150 ml in 1 bottle, dropper of Clofenax, a human prescription drug labeled by Puretek Corporation. The product's dosage form is kit and is administered via form.

    Is NDC 59088-727 included in the NDC Directory?

    Yes, Clofenax with product code 59088-727 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on December 09, 2020 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 59088-727-00?

    The 11-digit format is 59088072700. 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
    5-3-259088-727-005-4-259088-0727-00