Motion Sickness Relief Tablet
NDC Package 50844-199-02

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Motion Sickness Relief (dimenhydrinate) tablets is dimenhydrinate is an antihistamine used to prevent and treat nausea, vomiting and dizziness caused by motion sickness when medication cannot be given by mouth. This formulation utilizes a tablet delivery system. Marketed by L.n.k. International, Inc., this product is identified by NDC 50844-199 and is authorized under FDA application M009.

Identification & Billing

NDC Package Code
50844-199-02
Package Description
2 BLISTER PACK in 1 CARTON / 6 TABLET in 1 BLISTER PACK
Product Code
50844-199
11-Digit Billing Format
50844019902

Clinical Specifications

Proprietary Name
Motion Sickness Relief
Non-Proprietary Name
Dimenhydrinate
Substance Name
Dimenhydrinate
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
DIMENHYDRINATE 50 mg/1
Pharmacologic Class
Usage Information
Dimenhydrinate is an antihistamine used to prevent and treat nausea, vomiting and dizziness caused by motion sickness when medication cannot be given by mouth. Dimenhydrinate injection should not be used in newborns because of an increased risk of side effects.

Regulatory & Marketing

Labeler Name
L.n.k. International, Inc.
Product Type
Human Otc Drug
FDA Application #
M009
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-01-1992
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 50844-199-02 identifies a specific commercial package of 2 blister pack in 1 carton / 6 tablet in 1 blister pack of Motion Sickness Relief, a human over the counter drug labeled by L.n.k. International, Inc.. This tablet is formulated for oral use and contains dimenhydrinate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by L.n.k. International, Inc. on December 01, 1992. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

Dimenhydrinate is an antihistamine used to prevent and treat nausea, vomiting and dizziness caused by motion sickness when medication cannot be given by mouth. Dimenhydrinate injection should not be used in newborns because of an increased risk of side effects.

How is this L.n.k. International, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50844019902. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
50844-199-02
11-Digit CMS (5-4-2)
50844-0199-02

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.