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  5. NDC Package Code: 70934-224-30 Fenofibrate

NDC Package 70934-224-30 Fenofibrate

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:
70934-224-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
70934-224
Proprietary Name:
Fenofibrate
Usage Information:
Fenofibrate is used along with a proper diet to help lower "bad" cholesterol and fats (such as LDL, triglycerides) and raise "good" cholesterol (HDL) in the blood. It works by increasing the natural substance (enzyme) that breaks down fats in the blood. Fenofibrate belongs to a group of drugs known as "fibrates." Lowering triglycerides in people with very high triglyceride blood levels may decrease the risk of pancreas disease (pancreatitis). However, fenofibrate might not lower your risk of a heart attack or stroke. Talk to your doctor about the risks and benefits of fenofibrate. In addition to eating a proper diet (such as a low-cholesterol/low-fat diet), other lifestyle changes that may help this medication work better include exercising, losing weight if overweight, and stopping smoking. Consult your doctor for more details.
11-Digit NDC Billing Format:
70934022430
NDC to RxNorm Crosswalk:
  • RxCUI: 477560 - fenofibrate 145 MG Oral Tablet
    • Labeler Name:
    Denton Pharma, Inc. Dba Northwind Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    01-08-2019
    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 70934-224-30?

    The NDC Packaged Code 70934-224-30 is assigned to a package of 30 tablet, film coated in 1 bottle, plastic of Fenofibrate, labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 70934-224 included in the NDC Directory?

    No, Fenofibrate with product code 70934-224 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals on January 08, 2019 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 11-digit format for NDC 70934-224-30?

    The 11-digit format is 70934022430. 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
    5-3-270934-224-305-4-270934-0224-30