Scopolamine Patch
NDC Package 0378-6470-99

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

Package Information

Scopolamine patches is this skin patch is used to prevent nausea and vomiting caused by motion sickness or recovery from anesthesia and surgery. This formulation utilizes a patch delivery system. Marketed by Mylan Pharmaceuticals Inc., this product is identified by NDC 0378-6470 and is authorized under FDA application ANDA203753.

Identification & Billing

NDC Package Code
0378-6470-99
Package Description
4 POUCH in 1 CARTON / 1 PATCH in 1 POUCH (0378-6470-16) / 3 d in 1 PATCH
Product Code
0378-6470
11-Digit Billing Format
00378647099
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Scopolamine
Non-Proprietary Name
Scopolamine
Substance Name
Scopolamine
Dosage Form
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
Administration Route
Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Active Ingredient(s)
SCOPOLAMINE 1 mg/3d
Pharmacologic Class
Usage Information
This skin patch is used to prevent nausea and vomiting caused by motion sickness or recovery from anesthesia and surgery. This medication works by correcting the imbalance of natural substances (acetylcholine and norepinephrine) that can occur in motion sickness. It also blocks certain signals to the brain that can cause nausea and vomiting. This medication is not recommended for use in children.

Regulatory & Marketing

Labeler Name
Mylan Pharmaceuticals Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA203753
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
06-19-2019
Listing Expiration
12-31-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0378-6470). Click a package code to view its specific billing and regulatory data.

0378-6470-44
24 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 3 d in 1 PATCH
0378-6470-97
10 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 3 d in 1 PATCH

* 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 0378-6470-99 identifies a specific commercial package of 4 pouch in 1 carton / 1 patch in 1 pouch (0378-6470-16) / 3 d in 1 patch of Scopolamine, a human prescription drug labeled by Mylan Pharmaceuticals Inc.. This patch is formulated for transdermal use and contains scopolamine 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 Mylan Pharmaceuticals Inc. on June 19, 2019. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

This skin patch is used to prevent nausea and vomiting caused by motion sickness or recovery from anesthesia and surgery. This medication works by correcting the imbalance of natural substances (acetylcholine and norepinephrine) that can occur in motion sickness. It also blocks certain signals to the brain that can cause nausea and vomiting. This medication is not recommended for use in children.

How is this Mylan Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00378647099. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. 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 (4-4-2)
0378-6470-99
11-Digit CMS (5-4-2)
00378-6470-99

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