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  4. NDC Product Code: 55037-640 Oxygen/helium 50/50

NDC 55037-640 Oxygen/helium 50/50

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55037-640?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55037-640
Proprietary Name:
Oxygen/helium 50/50
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Matheson Tri-gas, Inc.
Labeler Code:
55037
Product Label ID:
d7c6329f-1dc8-b25c-e053-2a95a90a2452
Start Marketing Date: [9]
01-01-1987
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 55037-640?

The NDC code 55037-640 is assigned by the FDA to the product Oxygen/helium 50/50 which is product labeled by Matheson Tri-gas, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 55037-640-01 6010 l in 1 cylinder , 55037-640-02 650 l in 1 cylinder , 55037-640-03 630 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/helium 50/50 UNII Codes?

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

Which are Oxygen/helium 50/50 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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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".