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  5. NDC Package Code: 70859-058-01 Nudiclo Solupak

NDC Package 70859-058-01 Nudiclo Solupak

Diclofenac Sodium,Capsaicin 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:
70859-058-01
Package Description:
1 KIT in 1 KIT * 1 BOTTLE, DROPPER in 1 CARTON (51672-1358-2) / 150 mL in 1 BOTTLE, DROPPER * 1 TUBE in 1 CARTON (0536-2525-25) / 60 g in 1 TUBE
Product Code:
70859-058
Proprietary Name:
Nudiclo Solupak
Non-Proprietary Name:
Diclofenac Sodium, Capsaicin
Usage Information:
Diclofenac sodium topical solution is a nonsteroidal anti-inflammatory drug (NSAID) indicated for the treatment of signs and symptoms of osteoarthritis of the knee(s).
11-Digit NDC Billing Format:
70859005801
NDC to RxNorm Crosswalk:
  • RxCUI: 198555 - capsaicin 0.025 % Topical Cream
  • RxCUI: 198555 - capsaicin 0.25 MG/ML Topical Cream
  • 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
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Nucare Pharmaceuticals,inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    ANDA202769
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-08-2023
    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 70859-058-01?

    The NDC Packaged Code 70859-058-01 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 * 1 tube in 1 carton (0536-2525-25) / 60 g in 1 tube of Nudiclo Solupak, a human prescription drug labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is kit and is administered via form.

    Is NDC 70859-058 included in the NDC Directory?

    Yes, Nudiclo Solupak with product code 70859-058 is active and included in the NDC Directory. The product was first marketed by Nucare Pharmaceuticals,inc. on February 08, 2023 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 70859-058-01?

    The 11-digit format is 70859005801. 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
    5-3-270859-058-015-4-270859-0058-01