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  5. NDC Package Code: 70859-035-01 Nudroxipak E-400

NDC Package 70859-035-01 Nudroxipak E-400

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
70859-035-01
Package Description:
1 KIT in 1 CARTON * 1 CONTAINER in 1 CARTON (70859-028-03) / 90 mL in 1 CONTAINER * 100 TABLET, FILM COATED in 1 BOTTLE (60505-0041-1)
Product Code:
70859-035
Proprietary Name:
Nudroxipak E-400
Usage Information:
Carefully consider the potential benefits and risks of etodolac and other treatment options before deciding to use etodolac. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS). Etodolac tablets, USP are indicated:For acute and long-term use in the management of signs and symptoms of the following: Osteoarthritis Rheumatoid arthritis For the management of acute pain
11-Digit NDC Billing Format:
70859003501
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 197686 - etodolac 400 MG Oral Tablet
  • RxCUI: 1989491 - capsaicin 0.025 % / menthol 6 % / methyl salicylate 25 % Topical Solution
  • RxCUI: 1989491 - capsaicin 0.25 MG/ML / menthol 60 MG/ML / methyl salicylate 250 MG/ML Topical Solution
    • Labeler Name:
    Nucare Pharmaceuticals,inc.
    Sample Package:
    No
    Start Marketing Date:
    03-16-2018
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 70859-035-01?

    The NDC Packaged Code 70859-035-01 is assigned to a package of 1 kit in 1 carton * 1 container in 1 carton (70859-028-03) / 90 ml in 1 container * 100 tablet, film coated in 1 bottle (60505-0041-1) of Nudroxipak E-400, labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is and is administered via form.

    Is NDC 70859-035 included in the NDC Directory?

    No, Nudroxipak E-400 with product code 70859-035 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nucare Pharmaceuticals,inc. on March 16, 2018 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 70859-035-01?

    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 70859-035-01?

    The 11-digit format is 70859003501. 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
    5-3-270859-035-015-4-270859-0035-01