Nitrogen
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Nitrogen
- Generic name
- NITROGEN
- Manufacturer
- A-OX Welding Supply, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d810b2ee-0e0a-e952-e053-2a95a90afeca
- SPL ID
- 41d950b2-e0bd-97aa-e063-6294a90a996c
- Version
- 5
- Effective date
- 2025-10-23
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:51
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 205766 | derived:openfda.application_number |
| application number | NDA205766 | openfda.application_number | |
| brand name | Nitrogen | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | A-OX Welding Supply, LLC | openfda.manufacturer_name | |
| ndc | package | 10297-200-03 | openfda.package_ndc |
| ndc | package | 10297-200-05 | openfda.package_ndc |
| ndc | package | 10297-200-01 | openfda.package_ndc |
| ndc | package | 10297-200-11 | openfda.package_ndc |
| ndc | package | 10297-200-02 | openfda.package_ndc |
| ndc | package | 10297-200-06 | openfda.package_ndc |
| ndc | package | 10297-200-04 | openfda.package_ndc |
| ndc | package | 10297-200-08 | openfda.package_ndc |
| ndc | package | 10297-200-10 | openfda.package_ndc |
| ndc | package | 10297-200-09 | openfda.package_ndc |
| ndc | package | 10297-200-07 | openfda.package_ndc |
| ndc | product | 10297-200 | openfda.product_ndc |
| ndc11 | package | 10297020008 | derived:openfda.package_ndc |
| ndc11 | package | 10297020005 | derived:openfda.package_ndc |
| ndc11 | package | 10297020002 | derived:openfda.package_ndc |
| ndc11 | package | 10297020001 | derived:openfda.package_ndc |
| ndc11 | package | 10297020010 | derived:openfda.package_ndc |
| ndc11 | package | 10297020009 | derived:openfda.package_ndc |
| ndc11 | package | 10297020007 | derived:openfda.package_ndc |
| ndc11 | package | 10297020006 | derived:openfda.package_ndc |
| ndc11 | package | 10297020011 | derived:openfda.package_ndc |
| ndc11 | package | 10297020004 | derived:openfda.package_ndc |
| ndc11 | package | 10297020003 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 41d950b2-e0bd-97aa-e063-6294a90a996c | id | |
| spl set id | d810b2ee-0e0a-e952-e053-2a95a90afeca | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.