NDC 53620-101 Carbon Dioxide

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53620-101
Proprietary Name:
Carbon Dioxide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Esquire Gas Products Company, Inc
Labeler Code:
53620
Start Marketing Date: [9]
01-01-1955
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 53620-101-01

Package Description: 11500 L in 1 CYLINDER

NDC Code 53620-101-02

Package Description: 88320 L in 1 CYLINDER

NDC Code 53620-101-03

Package Description: 2760000 L in 1 TANK

NDC Code 53620-101-04

Package Description: 5520000 L in 1 TANK

NDC Code 53620-101-05

Package Description: 11040000 L in 1 TANK

Product Details

What is NDC 53620-101?

The NDC code 53620-101 is assigned by the FDA to the product Carbon Dioxide which is product labeled by Esquire Gas Products Company, Inc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 53620-101-01 11500 l in 1 cylinder , 53620-101-02 88320 l in 1 cylinder , 53620-101-03 2760000 l in 1 tank , 53620-101-04 5520000 l in 1 tank , 53620-101-05 11040000 l in 1 tank . 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 Carbon Dioxide UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Carbon Dioxide?

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".