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  5. NDC Package Code: 67877-390-01 Nebivolol

NDC Package 67877-390-01 Nebivolol

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
67877-390-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
67877-390
Proprietary Name:
Nebivolol
Non-Proprietary Name:
Nebivolol
Substance Name:
Nebivolol Hydrochloride
Usage Information:
Nebivolol is contraindicated in the following conditions:Severe bradycardiaHeart block greater than first degreePatients with cardiogenic shockDecompensated cardiac failureSick sinus syndrome (unless a permanent pacemaker is in place)Patients with severe hepatic impairment (Child-Pugh greater than B)Patients who are hypersensitive to any component of this product.
11-Digit NDC Billing Format:
67877039001
NDC to RxNorm Crosswalk:
  • RxCUI: 387013 - nebivolol 5 MG Oral Tablet
  • RxCUI: 387013 - nebivolol (as nebivolol hydrochloride) 5 MG Oral Tablet
  • RxCUI: 751612 - nebivolol 10 MG Oral Tablet
  • RxCUI: 751612 - nebivolol (as nebivolol hydrochloride) 10 MG Oral Tablet
  • RxCUI: 751618 - nebivolol 2.5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ascend Laboratories, Llc
    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):
  • NEBIVOLOL HYDROCHLORIDE 20 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:
    ANDA203828
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-16-2021
    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
    67877-390-3030 TABLET in 1 BOTTLE
    67877-390-331 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
    67877-390-9090 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67877-390-01?

    The NDC Packaged Code 67877-390-01 is assigned to a package of 100 tablet in 1 bottle of Nebivolol, a human prescription drug labeled by Ascend Laboratories, Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 67877-390 included in the NDC Directory?

    Yes, Nebivolol with product code 67877-390 is active and included in the NDC Directory. The product was first marketed by Ascend Laboratories, Llc on September 16, 2021 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 67877-390-01?

    The 11-digit format is 67877039001. 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
    5-3-267877-390-015-4-267877-0390-01