1. Labeler Index
  2. Gt Industries Inc
  3. NDC Product Code: 61095-200 Nitrogen

NDC 61095-200 Nitrogen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 61095-200?
    4. Active Ingredients UNII Codes
    5. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61095-200
Proprietary Name:
Nitrogen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gt Industries Inc
Labeler Code:
61095
Product Label ID:
013f400f-3795-41e7-b543-073c73f10675
Start Marketing Date: [9]
01-01-1994
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61095-200-01

Package Description: 7277 L in 1 CYLINDER

NDC Code 61095-200-02

Package Description: 651 L in 1 CYLINDER

Product Details

What is NDC 61095-200?

The NDC code 61095-200 is assigned by the FDA to the product Nitrogen which is product labeled by Gt Industries Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 61095-200-01 7277 l in 1 cylinder , 61095-200-02 651 l in 1 cylinder . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

Which are Nitrogen UNII Codes?

The UNII codes for the active ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Nitrogen?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".