NDC Package 29300-412-01 Atenolol

Tablet 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:
29300-412-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Atenolol
Non-Proprietary Name:
Atenolol
Substance Name:
Atenolol
Usage Information:
Atenolol is used with or without other medications to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This medication is also used to treat chest pain (angina) and to improve survival after a heart attack. Atenolol belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in your body, such as epinephrine, on the heart and blood vessels. This effect lowers the heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
29300041201
NDC to RxNorm Crosswalk:
  • RxCUI: 197379 - atenolol 100 MG Oral Tablet
  • RxCUI: 197380 - atenolol 25 MG Oral Tablet
  • RxCUI: 197381 - atenolol 50 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Unichem Pharmaceuticals (usa), Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA213136
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-21-2019
    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
    29300-412-05500 TABLET in 1 BOTTLE
    29300-412-101000 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 29300-412-01?

    The NDC Packaged Code 29300-412-01 is assigned to a package of 100 tablet in 1 bottle of Atenolol, a human prescription drug labeled by Unichem Pharmaceuticals (usa), Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 29300-412 included in the NDC Directory?

    Yes, Atenolol with product code 29300-412 is active and included in the NDC Directory. The product was first marketed by Unichem Pharmaceuticals (usa), Inc. on November 21, 2019 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 11-digit format for NDC 29300-412-01?

    The 11-digit format is 29300041201. 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
    5-3-229300-412-015-4-229300-0412-01