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  5. NDC Package Code: 63029-906-12 Dramamine

NDC Package 63029-906-12 Dramamine

Meclizine Hydrochloride 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:
63029-906-12
Package Description:
12 TABLET, CHEWABLE in 1 BLISTER PACK
Product Code:
63029-906
Proprietary Name:
Dramamine
Non-Proprietary Name:
Meclizine Hydrochloride
Substance Name:
Meclizine Hydrochloride
Usage Information:
■to prevent motion sickness take first dose ½ hour to 1 hour before activity that may result in nausea■to treat motion sickness, take at first signs of symptoms■adults and children 12 years and over: 1 to 2 tablets once daily, or as directed by a doctor
11-Digit NDC Billing Format:
63029090612
NDC to RxNorm Crosswalk:
  • RxCUI: 2176732 - Dramamine Less Drowsy 25 MG Chewable Tablet
  • RxCUI: 2176732 - meclizine hydrochloride 25 MG Chewable Tablet [Dramamine Less Drowsy]
  • RxCUI: 995632 - meclizine HCl 25 MG Chewable Tablet
  • RxCUI: 995632 - meclizine hydrochloride 25 MG Chewable Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Medtech Products Inc.
    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:
    part336
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    02-15-2019
    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.

    Frequently Asked Questions

    What is NDC 63029-906-12?

    The NDC Packaged Code 63029-906-12 is assigned to a package of 12 tablet, chewable in 1 blister pack of Dramamine, a human over the counter drug labeled by Medtech Products Inc.. The product's dosage form is tablet, chewable and is administered via oral form.

    Is NDC 63029-906 included in the NDC Directory?

    Yes, Dramamine with product code 63029-906 is active and included in the NDC Directory. The product was first marketed by Medtech Products Inc. on February 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 11-digit format for NDC 63029-906-12?

    The 11-digit format is 63029090612. 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
    5-3-263029-906-125-4-263029-0906-12