NDC Package 52536-133-01 Meclizine Hydrochloride

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

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:
52536-133-01
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
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.
11-Digit NDC Billing Format:
52536013301
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 995624 - meclizine HCl 12.5 MG Oral Tablet
  • RxCUI: 995624 - meclizine hydrochloride 12.5 MG Oral Tablet
  • RxCUI: 995666 - meclizine HCl 25 MG Oral Tablet
  • RxCUI: 995666 - meclizine hydrochloride 25 MG Oral Tablet
  • RxCUI: 995686 - meclizine HCl 50 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Wilshire 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):
    Sample Package:
    No
    FDA Application Number:
    ANDA205136
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-15-2019
    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
    52536-133-101000 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52536-133-01?

    The NDC Packaged Code 52536-133-01 is assigned to a package of 100 tablet in 1 bottle of Meclizine Hydrochloride, a human prescription drug labeled by Wilshire Pharmaceuticals Inc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 52536-133 included in the NDC Directory?

    Yes, Meclizine Hydrochloride with product code 52536-133 is active and included in the NDC Directory. The product was first marketed by Wilshire Pharmaceuticals Inc on April 15, 2019 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 NDC billing unit for package 52536-133-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

    What is the 11-digit format for NDC 52536-133-01?

    The 11-digit format is 52536013301. 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
    5-3-252536-133-015-4-252536-0133-01