NDC 64920-0001 Oxygen

Oxygen

NDC Product Code 64920-0001

NDC 64920-0001-2

Package Description: 170 L in 1 CYLINDER

NDC 64920-0001-3

Package Description: 246 L in 1 CYLINDER

NDC 64920-0001-4

Package Description: 415 L in 1 CYLINDER

NDC 64920-0001-5

Package Description: 662 L in 1 CYLINDER

NDC 64920-0001-6

Package Description: 1724 L in 1 CYLINDER

NDC 64920-0001-7

Package Description: 680 L in 1 CYLINDER

NDC Product Information

Oxygen with NDC 64920-0001 is a a human prescription drug product labeled by Whaba Medical, Inc.. The generic name of Oxygen is oxygen. The product's dosage form is gas and is administered via respiratory (inhalation) form.

Labeler Name: Whaba Medical, Inc.

Dosage Form: Gas - Any elastic aeriform fluid in which the molecules are separated from one another and so have free paths.

Product Type: Human Prescription Drug 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.

Oxygen Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • OXYGEN 99 L/100L

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.

Product Labeler Information

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

Labeler Name: Whaba Medical, Inc.
Labeler Code: 64920
Marketing Category: UNAPPROVED MEDICAL GAS - 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.

Start Marketing Date: 10-30-2009 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: 12-31-2021 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: N - NO 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".

* Please review the disclaimer below.