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  5. NDC Package Code: 71335-0353-4 Buprenorphine

NDC Package 71335-0353-4 Buprenorphine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
71335-0353-4
Package Description:
7 TABLET in 1 BOTTLE
Product Code:
71335-0353
Proprietary Name:
Buprenorphine
Usage Information:
This medication is used to help relieve severe ongoing pain (such as due to arthritis, chronic back pain). Buprenorphine belongs to a class of drugs known as opioid analgesics. It works in the brain to change how your body feels and responds to pain. The higher strengths of this drug (7.5, 10, 15, or 20 micrograms per hour patches) should be used only if you have been regularly taking moderate amounts of opioid pain medication. These strengths may cause overdose (even death) if used by a person who has not been regularly taking opioids. Do not use this medication to relieve pain that is mild or that will go away in a few days. This medication is not for occasional ("as needed") use.
11-Digit NDC Billing Format:
71335035304
Labeler Name:
Bryant Ranch Prepack
Sample Package:
No
FDA Application Number:
ANDA090819
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
02-19-2015
End Marketing Date:
04-26-2017
Listing Expiration Date:
04-26-2017
Exclude Flag:
D
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
71335-0353-160 TABLET in 1 BOTTLE
71335-0353-290 TABLET in 1 BOTTLE
71335-0353-330 TABLET in 1 BOTTLE
71335-0353-528 TABLET in 1 BOTTLE
71335-0353-61 TABLET in 1 BOTTLE
71335-0353-712 TABLET in 1 BOTTLE
71335-0353-8120 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71335-0353-4?

The NDC Packaged Code 71335-0353-4 is assigned to a package of 7 tablet in 1 bottle of Buprenorphine, labeled by Bryant Ranch Prepack. The product's dosage form is and is administered via form.

Is NDC 71335-0353 included in the NDC Directory?

No, Buprenorphine with product code 71335-0353 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Bryant Ranch Prepack on February 19, 2015 and its listing in the NDC Directory is set to expire on April 26, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-0353-4?

The 11-digit format is 71335035304. 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
5-4-171335-0353-45-4-271335-0353-04