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  5. NDC Package Code: 70934-832-90 Pravastatin Sodium

NDC Package 70934-832-90 Pravastatin Sodium

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:
70934-832-90
Package Description:
90 TABLET in 1 BOTTLE, PLASTIC
Product Code:
70934-832
Proprietary Name:
Pravastatin Sodium
Usage Information:
Pravastatin 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 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. Consult your doctor for more details.
11-Digit NDC Billing Format:
70934083290
NDC to RxNorm Crosswalk:
  • RxCUI: 904475 - pravastatin sodium 40 MG Oral Tablet
    • Labeler Name:
    Denton Pharma, Inc. Dba Northwind Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    03-23-2021
    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 70934-832-90?

    The NDC Packaged Code 70934-832-90 is assigned to a package of 90 tablet in 1 bottle, plastic of Pravastatin Sodium, labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 70934-832 included in the NDC Directory?

    No, Pravastatin Sodium with product code 70934-832 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 March 23, 2021 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 70934-832-90?

    The 11-digit format is 70934083290. 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
    5-3-270934-832-905-4-270934-0832-90