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  5. NDC Package Code: 49873-805-01 Zentrip Motion Sickness

NDC Package 49873-805-01 Zentrip Motion Sickness

Meclizine Hydrochloride 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:
49873-805-01
Package Description:
2 BLISTER PACK in 1 BOX / 6 TABLET in 1 BLISTER PACK
Product Code:
49873-805
Proprietary Name:
Zentrip Motion Sickness
Non-Proprietary Name:
Meclizine Hydrochloride
Substance Name:
Meclizine Hydrochloride
Usage Information:
To prevent motion sickness, take it at least one hour before travelingadults and children 12 years of age and over: take 1 to 2 tablets (25 to 50mg) once daily, or as directed by a physician.
11-Digit NDC Billing Format:
49873080501
NDC to RxNorm Crosswalk:
  • RxCUI: 1663815 - meclizine HCl 25 MG Disintegrating Oral Tablet
  • RxCUI: 1663815 - meclizine hydrochloride 25 MG Disintegrating Oral Tablet
  • RxCUI: 2540687 - ZenTrip 25 MG Disintegrating Oral Tablet
  • RxCUI: 2540687 - meclizine hydrochloride 25 MG Disintegrating Oral Tablet [Zentrip]
  • RxCUI: 2540687 - Zentrip 25 MG Disintegrating Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Sato Pharmaceutical Co., Ltd
    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:
    M009
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-01-2021
    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 49873-805-01?

    The NDC Packaged Code 49873-805-01 is assigned to a package of 2 blister pack in 1 box / 6 tablet in 1 blister pack of Zentrip Motion Sickness, a human over the counter drug labeled by Sato Pharmaceutical Co., Ltd. The product's dosage form is tablet and is administered via oral form.

    Is NDC 49873-805 included in the NDC Directory?

    Yes, Zentrip Motion Sickness with product code 49873-805 is active and included in the NDC Directory. The product was first marketed by Sato Pharmaceutical Co., Ltd on May 01, 2021 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 49873-805-01?

    The 11-digit format is 49873080501. 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
    5-3-249873-805-015-4-249873-0805-01