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  5. NDC Package Code: 76282-349-01 Nadolol

NDC Package 76282-349-01 Nadolol

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
76282-349-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
76282-349
Proprietary Name:
Nadolol
Non-Proprietary Name:
Nadolol
Substance Name:
Nadolol
Usage Information:
Nadolol is used alone or with other medications to treat high blood pressure (hypertension) and to prevent chest pain (angina). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. In the management of chest pain, nadolol may also help to reduce the frequency of chest pain episodes and improve your ability to exercise. Nadolol belongs to a class of medications called beta blockers. It works by blocking the action of certain natural substances such as adrenaline (epinephrine) on the heart and blood vessels. This results in a lowering of heart rate, blood pressure, and strain on the heart.
11-Digit NDC Billing Format:
76282034901
NDC to RxNorm Crosswalk:
  • RxCUI: 198006 - nadolol 20 MG Oral Tablet
  • RxCUI: 198007 - nadolol 40 MG Oral Tablet
  • RxCUI: 198008 - nadolol 80 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Exelan Pharmaceuticals 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):
  • NADOLOL 80 mg/1
    • Pharmacologic Class(es):
  • Adrenergic beta-Antagonists - [MoA] (Mechanism of Action)
  • beta-Adrenergic Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA203455
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-27-2020
    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.

    Frequently Asked Questions

    What is NDC 76282-349-01?

    The NDC Packaged Code 76282-349-01 is assigned to a package of 100 tablet in 1 bottle of Nadolol, a human prescription drug labeled by Exelan Pharmaceuticals Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 76282-349 included in the NDC Directory?

    Yes, Nadolol with product code 76282-349 is active and included in the NDC Directory. The product was first marketed by Exelan Pharmaceuticals Inc. on July 27, 2020 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 76282-349-01?

    The 11-digit format is 76282034901. 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
    5-3-276282-349-015-4-276282-0349-01