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  5. NDC Package Code: 49467-124-16 Naus-ease

NDC Package 49467-124-16 Naus-ease

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:
49467-124-16
Package Description:
2 BLISTER PACK in 1 CARTON / 8 TABLET in 1 BLISTER PACK
Product Code:
49467-124
Proprietary Name:
Naus-ease
Non-Proprietary Name:
Meclizine Hydrochloride
Substance Name:
Meclizine Hydrochloride
Usage Information:
For Consumers (the general public):Naus-Ease® (Meclizine Hydrochloride), USP Tablets are used for the prevention and treatment of nausea and vomiting, or dizziness associated with motion sickness.For Health Professionals:Based on a review of Meclizine Hydrochloride, USP drug by the National Academy of Sciences – National Research Council and/or other information, FDA has classified the indications of Meclizine Hydrochloride, USP as follows: 1. The prevention and treatment (management) of nausea and vomiting, and dizziness associated with motion sickness. 2. For the treatment of vertigo.
11-Digit NDC Billing Format:
49467012416
NDC to RxNorm Crosswalk:
  • RxCUI: 1372663 - Naus-Ease 25 MG Oral Tablet
  • RxCUI: 1372663 - meclizine hydrochloride 25 MG Oral Tablet [Naus-ease]
  • RxCUI: 1372663 - Naus-ease 25 MG Oral Tablet
  • RxCUI: 995666 - meclizine HCl 25 MG Oral Tablet
  • RxCUI: 995666 - meclizine hydrochloride 25 MG Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Sunascen Therapeutics 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):
  • MECLIZINE HYDROCHLORIDE 25 mg/1
    • Pharmacologic Class(es):
  • Antiemetic - [EPC] (Established Pharmacologic Class)
  • Emesis Suppression - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA040659
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-16-2012
    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
    49467-124-081 BLISTER PACK in 1 CARTON / 8 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 49467-124-16?

    The NDC Packaged Code 49467-124-16 is assigned to a package of 2 blister pack in 1 carton / 8 tablet in 1 blister pack of Naus-ease, a human over the counter drug labeled by Sunascen Therapeutics Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 49467-124 included in the NDC Directory?

    Yes, Naus-ease with product code 49467-124 is active and included in the NDC Directory. The product was first marketed by Sunascen Therapeutics Llc on April 16, 2012 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 49467-124-16?

    The 11-digit format is 49467012416. 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
    5-3-249467-124-165-4-249467-0124-16