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  5. NDC Package Code: 80136-779-01 Meclizine Hydrochloride

NDC Package 80136-779-01 Meclizine Hydrochloride

Meclizine Hcl Tablet, Chewable 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:
80136-779-01
Package Description:
100 TABLET, CHEWABLE in 1 BOTTLE
Product Code:
80136-779
Proprietary Name:
Meclizine Hydrochloride
Non-Proprietary Name:
Meclizine Hcl
Substance Name:
Meclizine Hydrochloride
Usage Information:
Meclizine is an antihistamine that is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It may also be used to reduce dizziness and loss of balance (vertigo) caused by inner ear problems.
11-Digit NDC Billing Format:
80136077901
NDC to RxNorm Crosswalk:
  • RxCUI: 995632 - meclizine HCl 25 MG Chewable Tablet
  • RxCUI: 995632 - meclizine hydrochloride 25 MG Chewable Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Northeast Pharma
    Dosage Form:
    Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • MECLIZINE HYDROCHLORIDE 25 mg/1
    • Pharmacologic Class(es):
  • Antiemetic - [EPC] (Established Pharmacologic Class)
  • Emesis Suppression - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    M009
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-01-2022
    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.

    Frequently Asked Questions

    What is NDC 80136-779-01?

    The NDC Packaged Code 80136-779-01 is assigned to a package of 100 tablet, chewable in 1 bottle of Meclizine Hydrochloride, a human over the counter drug labeled by Northeast Pharma. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 80136-779 included in the NDC Directory?

    Yes, Meclizine Hydrochloride with product code 80136-779 is active and included in the NDC Directory. The product was first marketed by Northeast Pharma on November 01, 2022 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 80136-779-01?

    The 11-digit format is 80136077901. 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
    5-3-280136-779-015-4-280136-0779-01