NDC Package 42571-202-05 Olmesartan Medoxomil

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:
42571-202-05
Package Description:
500 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Olmesartan Medoxomil
Non-Proprietary Name:
Olmesartan Medoxomil
Substance Name:
Olmesartan Medoxomil
Usage Information:
Olmesartan is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. Olmesartan belongs to a class of drugs called angiotensin receptor blockers (ARBs). It works by relaxing blood vessels so that blood can flow more easily.
11-Digit NDC Billing Format:
42571020205
NDC to RxNorm Crosswalk:
  • RxCUI: 349373 - olmesartan medoxomil 5 MG Oral Tablet
  • RxCUI: 349401 - olmesartan medoxomil 20 MG Oral Tablet
  • RxCUI: 349405 - olmesartan medoxomil 40 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Micro Labs Limited
    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:
    ANDA206372
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-03-2020
    Listing Expiration Date:
    12-31-2024
    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
    42571-202-101000 TABLET, FILM COATED in 1 BOTTLE
    42571-202-1110 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK (42571-202-32)
    42571-202-3030 TABLET, FILM COATED in 1 BOTTLE
    42571-202-9090 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 42571-202-05?

    The NDC Packaged Code 42571-202-05 is assigned to a package of 500 tablet, film coated in 1 bottle of Olmesartan Medoxomil, a human prescription drug labeled by Micro Labs Limited. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 42571-202 included in the NDC Directory?

    Yes, Olmesartan Medoxomil with product code 42571-202 is active and included in the NDC Directory. The product was first marketed by Micro Labs Limited on February 03, 2020 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 42571-202-05?

    The 11-digit format is 42571020205. 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
    5-3-242571-202-055-4-242571-0202-05