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  5. NDC Package Code: 70007-400-12 Gonitro

NDC Package 70007-400-12 Gonitro

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 inactivated by the FDA.

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:
70007-400-12
Package Description:
12 PACKET in 1 BOX / 1 POWDER in 1 PACKET (70007-400-01)
Product Code:
70007-400
Proprietary Name:
Gonitro
Usage Information:
This medication is used to relieve chest pain (angina) in people that have a certain heart condition (coronary artery disease). It may also be used before physical activities (such as exercise, sexual activity) to help prevent chest pain. Nitroglycerin belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enough blood. This drug works by relaxing and widening blood vessels so blood can flow more easily to the heart.
11-Digit NDC Billing Format:
70007040012
NDC to RxNorm Crosswalk:
  • RxCUI: 1799428 - nitroglycerin 400 MCG Sublingual Powder
  • RxCUI: 1799428 - nitroglycerin 0.4 MG Sublingual Powder
  • RxCUI: 1799428 - NTG 0.4 MG Sublingual Powder
  • RxCUI: 1799428 - TNG 0.4 MG Sublingual Powder
  • RxCUI: 1799434 - GONITRO 400 MCG Sublingual Powder
    • Labeler Name:
    Espero Pharmaceuticals, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-01-2016
    Listing Expiration Date:
    12-31-2019
    Exclude Flag:
    I
    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
    70007-400-3636 PACKET in 1 BOX / 1 POWDER in 1 PACKET
    70007-400-9696 PACKET in 1 BOX / 1 POWDER in 1 PACKET
    70007-400-993 PACKET in 1 BOX / 1 POWDER in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70007-400-12?

    The NDC Packaged Code 70007-400-12 is assigned to a package of 12 packet in 1 box / 1 powder in 1 packet (70007-400-01) of Gonitro, labeled by Espero Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 70007-400 included in the NDC Directory?

    No, Gonitro with product code 70007-400 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Espero Pharmaceuticals, Inc. on July 01, 2016 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70007-400-12?

    The 11-digit format is 70007040012. 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 5-3-2 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
    5-3-270007-400-125-4-270007-0400-12