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  4. NDC Product Code: 68624-001 Oxygen

NDC 68624-001 Oxygen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68624-001?
  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.

Get all the details for National Drug Code (NDC) 68624-001 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
68624-001
Proprietary Name:
Oxygen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tech Air Of Naugatuck Llc
Labeler Code:
68624
Product Label ID:
04348084-7460-468b-aaf4-77dd6908d31a
Marketing Category: [8]
UNAPPROVED MEDICAL GAS - A category specifying that a product is marketed as unapproved medical gas.
Start Marketing Date: [9]
01-01-2004
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 68624-001?

The NDC code 68624-001 is assigned by the FDA to the product Oxygen which is product labeled by Tech Air Of Naugatuck Llc. The product's dosage form is . The product is distributed in 20 packages with assigned NDC codes 68624-001-01 102 l in 1 cylinder , 68624-001-02 141 l in 1 cylinder , 68624-001-03 149 l in 1 cylinder , 68624-001-04 178 l in 1 cylinder , 68624-001-05 234 l in 1 cylinder , 68624-001-06 387 l in 1 cylinder , 68624-001-07 643 l in 1 cylinder , 68624-001-08 1699 l in 1 cylinder , 68624-001-09 2350 l in 1 cylinder , 68624-001-10 3540 l in 1 cylinder , 68624-001-11 3511 l in 1 cylinder , 68624-001-12 4361 l in 1 cylinder , 68624-001-13 7100 l in 1 cylinder , 68624-001-14 9401 l in 1 cylinder , 68624-001-15 102 l in 1 cylinder , 68624-001-16 149 l in 1 cylinder , 68624-001-17 178 l in 1 cylinder , 68624-001-18 141159 l in 1 cylinder , 68624-001-19 145973 l in 1 cylinder , 68624-001-20 137053 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 Oxygen UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Oxygen?

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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".