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  5. NDC Package Code: 71335-9619-6 Meclizine Hydrochloride

NDC Package 71335-9619-6 Meclizine Hydrochloride

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:
71335-9619-6
Package Description:
60 TABLET in 1 BOTTLE
Product Code:
71335-9619
Proprietary Name:
Meclizine Hydrochloride
Non-Proprietary Name:
Meclizine Hydrochloride
Substance Name:
Meclizine Hydrochloride
Usage Information:
Meclizine hydrochloride tablets are indicated for the treatment of vertigo associated with diseases affecting the vestibular system in adults.
11-Digit NDC Billing Format:
71335961906
NDC to RxNorm Crosswalk:
  • RxCUI: 995666 - meclizine HCl 25 MG Oral Tablet
  • RxCUI: 995666 - meclizine hydrochloride 25 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bryant Ranch Prepack
    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):
  • MECLIZINE HYDROCHLORIDE 25 mg/1
    • Pharmacologic Class(es):
  • Antiemetic - [EPC] (Established Pharmacologic Class)
  • Emesis Suppression - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA084657
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-27-2021
    End Marketing Date:
    10-31-2024
    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
    71335-9619-014 TABLET in 1 BOTTLE
    71335-9619-190 TABLET in 1 BOTTLE
    71335-9619-230 TABLET in 1 BOTTLE
    71335-9619-325 TABLET in 1 BOTTLE
    71335-9619-420 TABLET in 1 BOTTLE
    71335-9619-540 TABLET in 1 BOTTLE
    71335-9619-7120 TABLET in 1 BOTTLE
    71335-9619-810 TABLET in 1 BOTTLE
    71335-9619-9100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71335-9619-6?

    The NDC Packaged Code 71335-9619-6 is assigned to a package of 60 tablet in 1 bottle of Meclizine Hydrochloride, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is tablet and is administered via oral form.

    Is NDC 71335-9619 included in the NDC Directory?

    Yes, Meclizine Hydrochloride with product code 71335-9619 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on December 27, 2021.

    What is the 11-digit format for NDC 71335-9619-6?

    The 11-digit format is 71335961906. 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
    5-4-171335-9619-65-4-271335-9619-06