NDC Package 70859-004-01 Nudiclo Tabpak

Diclofenac Sodium,Capsaicin Kit - 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:
70859-004-01
Package Description:
1 KIT in 1 CARTON * 60 TABLET, DELAYED RELEASE in 1 BOTTLE (0228-2551-06) * 1 TUBE in 1 CARTON (0536-2525-25) / 60 g in 1 TUBE
Product Code:
Proprietary Name:
Nudiclo Tabpak
Non-Proprietary Name:
Diclofenac Sodium, Capsaicin
Usage Information:
Carefully consider the potential benefits and risks of diclofenac sodium delayed-release tablets, USP and other treatment options before deciding to use diclofenac sodium delayed-release tablets, USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS). Diclofenac sodium delayed-release tablets are indicated:For relief of the signs and symptoms of osteoarthritisFor relief of the signs and symptoms of rheumatoid arthritisFor acute or long-term use in the relief of signs and symptoms of ankylosing spondylitis
11-Digit NDC Billing Format:
70859000401
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 198555 - capsaicin 0.025 % Topical Cream
  • RxCUI: 198555 - capsaicin 0.25 MG/ML Topical Cream
  • RxCUI: 855926 - diclofenac sodium 75 MG Delayed Release Oral Tablet
  • 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:
    ANDA074514
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-26-2016
    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 70859-004-01?

    The NDC Packaged Code 70859-004-01 is assigned to a package of 1 kit in 1 carton * 60 tablet, delayed release in 1 bottle (0228-2551-06) * 1 tube in 1 carton (0536-2525-25) / 60 g in 1 tube of Nudiclo Tabpak, a human prescription drug labeled by Nucare Pharmaceuticals Inc. The product's dosage form is kit and is administered via form.

    Is NDC 70859-004 included in the NDC Directory?

    Yes, Nudiclo Tabpak with product code 70859-004 is active and included in the NDC Directory. The product was first marketed by Nucare Pharmaceuticals Inc on July 26, 2016 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 70859-004-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 70859-004-01?

    The 11-digit format is 70859000401. 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
    5-3-270859-004-015-4-270859-0004-01