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  5. NDC Package Code: 52959-629-30 Crestor

NDC Package 52959-629-30 Crestor

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:
52959-629-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
52959-629
Proprietary Name:
Crestor
Usage Information:
Rosuvastatin 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 belongs to a group of drugs known as "statins." It works by reducing the amount of cholesterol made by the liver. Lowering "bad" cholesterol and triglycerides and raising "good" cholesterol decreases the risk of heart disease and helps to prevent strokes and heart attacks. 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. Talk with your doctor for more details.
11-Digit NDC Billing Format:
52959062930
NDC to RxNorm Crosswalk:
  • RxCUI: 859751 - rosuvastatin calcium 20 MG Oral Tablet
  • RxCUI: 859753 - CRESTOR 20 MG Oral Tablet
  • RxCUI: 859753 - rosuvastatin calcium 20 MG Oral Tablet [Crestor]
  • RxCUI: 859753 - Crestor 20 MG Oral Tablet
    • Labeler Name:
    H.j. Harkins Company, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-21-2011
    Listing Expiration Date:
    12-31-2018
    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 52959-629-30?

    The NDC Packaged Code 52959-629-30 is assigned to a package of 30 tablet, film coated in 1 bottle of Crestor, labeled by H.j. Harkins Company, Inc.. The product's dosage form is and is administered via form.

    Is NDC 52959-629 included in the NDC Directory?

    No, Crestor with product code 52959-629 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by H.j. Harkins Company, Inc. on July 21, 2011 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52959-629-30?

    The 11-digit format is 52959062930. 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
    5-3-252959-629-305-4-252959-0629-30