NITROGEN Compressed, NF is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Airgas Usa, Llc. The primary component is Nitrogen.
Product ID | 11054-005_174de81b-3cef-4fe8-baf0-ee9c3e45204d |
NDC | 11054-005 |
Product Type | Human Prescription Drug |
Proprietary Name | NITROGEN Compressed, NF |
Generic Name | Nitrogen |
Dosage Form | Gas |
Route of Administration | RESPIRATORY (INHALATION) |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA / NDA |
Application Number | NDA205839 |
Labeler Name | AIRGAS USA, LLC |
Substance Name | NITROGEN |
Active Ingredient Strength | 992 mL/L |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 1997-11-06 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Marketing Category | NDA |
Application Number | NDA205839 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-11-06 |
Ingredient | Strength |
---|---|
NITROGEN | 992 mL/L |
SPL SET ID: | 6638a09f-7d87-48ce-934b-5edb3891ad61 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
11054-005 | NITROGEN Compressed, NF | NITROGEN Compressed, NF |
10006-005 | NITROGEN | NITROGEN |
10014-002 | Nitrogen | Nitrogen |
10018-9502 | Nitrogen | Nitrogen |
10167-400 | NITROGEN | NITROGEN |
10218-102 | NITROGEN | NITROGEN |
10221-002 | NITROGEN | NITROGEN |
10252-002 | Nitrogen | Nitrogen |
10297-002 | Nitrogen | Nitrogen |
10297-200 | Nitrogen | Nitrogen |
10304-601 | Nitrogen | Nitrogen |
10412-0095 | NITROGEN | NITROGEN |
10451-003 | Nitrogen | Nitrogen |
Mark Image Registration | Serial | Company Trademark Application Date |
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Raffles Investments (Proprietary) Limited 2018-02-04 |
NITROGEN 87478016 not registered Dead/Abandoned |
NITROGEN INTERNATIONAL LTD. 2017-06-07 |
NITROGEN 86224615 4839264 Live/Registered |
CYCLES ARGON-18 INC. 2014-03-18 |
NITROGEN 78592715 3114002 Live/Registered |
JB INTERNATIONAL HOLDINGS LIMITED 2005-03-22 |
NITROGEN 77961992 4527370 Live/Registered |
Huntsworth plc 2010-03-18 |
NITROGEN 77449738 3592799 Live/Registered |
Jay-Y Enterprise Co., Inc. 2008-04-16 |
NITROGEN 75759202 not registered Dead/Abandoned |
PROLAB NUTRTION, INC. 1999-07-23 |