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  5. NDC Package Code: 71335-2718-1 Scopolamine Transdermal System

NDC Package 71335-2718-1 Scopolamine Transdermal System

Patch, Extended Release Transdermal - 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:
71335-2718-1
Package Description:
10 POUCH in 1 CARTON / 1 PATCH, EXTENDED RELEASE in 1 POUCH
Product Code:
71335-2718
Proprietary Name:
Scopolamine Transdermal System
Non-Proprietary Name:
Scopolamine Transdermal System
Substance Name:
Scopolamine
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.
11-Digit NDC Billing Format:
71335271801
Product Type:
Human Prescription Drug
Labeler Name:
Bryant Ranch Prepack
Dosage Form:
Patch, Extended Release - A drug delivery system in the form of a patch that releases the drug in such a manner that a reduction in dosing frequency compared to that drug presented as a conventional dosage form (e.g., a solution or a prompt drug-releasing, conventional solid dosage form).
Administration Route(s):
Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Active Ingredient(s):
SCOPOLAMINE 1 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA078830
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-13-2017
Listing Expiration Date:
12-31-2026
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 71335-2718-1?

The NDC Packaged Code 71335-2718-1 is assigned to a package of 10 pouch in 1 carton / 1 patch, extended release in 1 pouch of Scopolamine Transdermal System, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is patch, extended release and is administered via transdermal form.

Is NDC 71335-2718 included in the NDC Directory?

Yes, Scopolamine Transdermal System with product code 71335-2718 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on June 13, 2017 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-2718-1?

The 11-digit format is 71335271801. 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 5-4-1 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
5-4-171335-2718-15-4-271335-2718-01