NDC Package 25208-202-15 Zypitamag

Pitavastatin Magnesium Tablet, Film Coated Oral - 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:
25208-202-15
Package Description:
500 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Zypitamag
Non-Proprietary Name:
Pitavastatin Magnesium
Substance Name:
Pitavastatin
Usage Information:
Pitavastatin 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:
25208020215
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
500 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2001262 - pitavastatin magnesium 2 MG Oral Tablet
  • RxCUI: 2001262 - pitavastatin 2 MG (as pitavastatin magnesium 2.053 MG) Oral Tablet
  • RxCUI: 2001264 - Zypitamag 2 MG Oral Tablet
  • RxCUI: 2001264 - pitavastatin magnesium 2 MG Oral Tablet [Zypitamag]
  • RxCUI: 2001264 - Zypitamag 2 MG (as pitavastatin magnesium 2.053 MG) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Medicure International Inc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA208379
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    03-09-2018
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    25208-202-0990 TABLET, FILM COATED in 1 BOTTLE
    25208-202-101 BLISTER PACK in 1 CARTON / 7 TABLET, FILM COATED in 1 BLISTER PACK
    25208-202-111000 TABLET, FILM COATED in 1 BOTTLE
    25208-202-1210 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
    25208-202-1330 TABLET, FILM COATED in 1 BOTTLE
    25208-202-14100 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 25208-202-15?

    The NDC Packaged Code 25208-202-15 is assigned to a package of 500 tablet, film coated in 1 bottle of Zypitamag, a human prescription drug labeled by Medicure International Inc. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 500 billable units per package.

    Is NDC 25208-202 included in the NDC Directory?

    Yes, Zypitamag with product code 25208-202 is active and included in the NDC Directory. The product was first marketed by Medicure International Inc on March 09, 2018 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 25208-202-15?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 500.

    What is the 11-digit format for NDC 25208-202-15?

    The 11-digit format is 25208020215. 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
    5-3-225208-202-155-4-225208-0202-15