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  5. NDC Package Code: 70518-3527-0 Nebivolol

NDC Package 70518-3527-0 Nebivolol

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:
70518-3527-0
Package Description:
90 TABLET in 1 BOTTLE, PLASTIC
Product Code:
70518-3527
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:
70518352700
NDC to RxNorm Crosswalk:
  • RxCUI: 387013 - nebivolol 5 MG Oral Tablet
  • RxCUI: 387013 - nebivolol (as nebivolol hydrochloride) 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack 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):
  • NEBIVOLOL HYDROCHLORIDE 5 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:
    09-20-2022
    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 70518-3527-0?

    The NDC Packaged Code 70518-3527-0 is assigned to a package of 90 tablet in 1 bottle, plastic of Nebivolol, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70518-3527 included in the NDC Directory?

    Yes, Nebivolol with product code 70518-3527 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on September 20, 2022 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 70518-3527-0?

    The 11-digit format is 70518352700. 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 5-4-1 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
    5-4-170518-3527-05-4-270518-3527-00