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  5. NDC Package Code: 70518-2718-1 Naltrexone Hydrochloride

NDC Package 70518-2718-1 Naltrexone Hydrochloride

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
70518-2718-1
Package Description:
28 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
70518-2718
Proprietary Name:
Naltrexone Hydrochloride
Non-Proprietary Name:
Naltrexone Hydrochloride
Substance Name:
Naltrexone Hydrochloride
Usage Information:
Naltrexone hydrochloride tablets are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. Naltrexone hydrochloride has not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions.
11-Digit NDC Billing Format:
70518271801
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Remedyrepack Inc.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
NALTREXONE HYDROCHLORIDE 50 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA090356
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
05-01-2020
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
70518-2718-030 TABLET, FILM COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70518-2718-1?

The NDC Packaged Code 70518-2718-1 is assigned to a package of 28 tablet, film coated in 1 blister pack of Naltrexone Hydrochloride, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 70518-2718 included in the NDC Directory?

Yes, Naltrexone Hydrochloride with product code 70518-2718 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on May 01, 2020 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 70518-2718-1?

The 11-digit format is 70518271801. 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
5-4-170518-2718-15-4-270518-2718-01