NDC 68419-0001 Oxygen
NDC Product Code 68419-0001
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
- 68419 - American Medical Gas Llc
NDC 68419-0001-1
Package Description: 170 L in 1 CYLINDER
NDC 68419-0001-2
Package Description: 248 L in 1 CYLINDER
NDC 68419-0001-3
Package Description: 415 L in 1 CYLINDER
NDC 68419-0001-4
Package Description: 682 L in 1 CYLINDER
NDC 68419-0001-5
Package Description: 3455 L in 1 CYLINDER
NDC 68419-0001-6
Package Description: 6910 L in 1 CYLINDER
NDC 68419-0001-7
Package Description: 41 L in 1 DEWAR
NDC 68419-0001-8
Package Description: 46 L in 1 DEWAR
NDC 68419-0001-9
Package Description: 31 L in 1 DEWAR
NDC Product Information
Oxygen with NDC 68419-0001 is a product labeled by American Medical Gas Llc. The generic name of Oxygen is . The product's dosage form is and is administered via form.
Labeler Name: American Medical Gas Llc
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: American Medical Gas Llc
Labeler Code: 68419
Start Marketing Date: 10-01-2003 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: 12-31-2017 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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