NDC 64540-001 Oxygen

  1. Labeler Index
  2. Austin Respiratory Equipment,inc.
  3. NDC: 64540-001 Oxygen

NDC Product Code 64540-001

NDC CODE: 64540-001

Proprietary Name: Oxygen What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 64540-001-01

Package Description: 170 L in 1 CYLINDER

NDC 64540-001-02

Package Description: 255 L in 1 CYLINDER

NDC 64540-001-03

Package Description: 450 L in 1 CYLINDER

NDC 64540-001-04

Package Description: 680 L in 1 CYLINDER

NDC 64540-001-05

Package Description: 1738 L in 1 CYLINDER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Oxygen with NDC 64540-001 is a product labeled by Austin Respiratory Equipment,inc.. The generic name of Oxygen is . The product's dosage form is and is administered via form.

Labeler Name: Austin Respiratory Equipment,inc.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Product Labeler Information

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

Labeler Name: Austin Respiratory Equipment,inc.
Labeler Code: 64540
Start Marketing Date: 07-11-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2018 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.
Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

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Oxygen Product Label Images