Oxygen, Refrigerated is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Airgas Usa, Llc. The primary component is Oxygen.
Product ID | 11054-010_0067712f-e6f6-4c8d-bf1f-17a20c0fd005 |
NDC | 11054-010 |
Product Type | Human Prescription Drug |
Proprietary Name | Oxygen, Refrigerated |
Generic Name | Oxygen, Refrigerated |
Dosage Form | Gas |
Route of Administration | RESPIRATORY (INHALATION) |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA / NDA |
Application Number | NDA205840 |
Labeler Name | AIRGAS USA, LLC |
Substance Name | OXYGEN |
Active Ingredient Strength | 992 mL/L |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 1997-10-14 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-01-17 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Marketing End Date | 2014-09-22 |
Marketing Category | NDA |
Application Number | NDA205840 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-10-14 |
Ingredient | Strength |
---|---|
OXYGEN | 992 mL/L |
SPL SET ID: | a22a66f6-33bb-4b1a-b6ee-bea3e5e634d8 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
11054-010 | Oxygen, Refrigerated | Oxygen, Refrigerated |
27190-100 | OXYGEN, REFRIGERATED | OXYGEN |
42545-000 | OXYGEN, REFRIGERATED | OXYGEN |
52472-100 | Oxygen, Refrigerated | OXYGEN |