72718-123 NDC - OXYGEN

Drug Information

Product NDC: 72718-123
Proprietary Name: Oxygen
Non Proprietary Name: Oxygen
Active Ingredient(s): 99 L/100L OXYGEN
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): GAS

Labeler Information

Field Name	Field Value
Labeler Name:	Surgimed Corporation
Product Type:	HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED MEDICAL GAS
Start Marketing Date:	5/9/2017

Package Information

No.	Package Code	Package Description	Billing Unit
1	72718-123-01	164 L in 1 CYLINDER (72718-123-01)
2	72718-123-02	255 L in 1 CYLINDER (72718-123-02)
3	72718-123-03	425 L in 1 CYLINDER (72718-123-03)
4	72718-123-04	680 L in 1 CYLINDER (72718-123-04)
5	72718-123-05	3455 L in 1 CYLINDER (72718-123-05)
6	72718-123-06	7080 L in 1 CYLINDER (72718-123-06)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	72718-123	This is the date that the labeler indicates was the start of its marketing of the drug product.
PRODUCT TYPE NAME	HUMAN PRESCRIPTION DRUG	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.
PROPRIETARY NAME	Oxygen	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
NON PROPRIETARY NAME	Oxygen	Name of Company corresponding to the labeler code segment of the Product NDC.
DOSAGE FORM NAME	GAS	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	RESPIRATORY (INHALATION)	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	5/9/2017	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED MEDICAL GAS	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.
LABELER NAME	Surgimed Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	OXYGEN	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	99
ACTIVE INGRED UNIT	L/100L

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This page was last updated on: 12/6/2025

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