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
- Jackson Welding Supply Co Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7c242f6e-06a9-44cd-8aec-2d90ece44f44
- SPL ID
- 40c02ca0-e79e-0920-e063-6394a90af7f0
- Version
- 13
- Effective date
- 2025-10-09
- Source export date
- 2026-11-06
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:42:28
| 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 | Jackson Welding Supply Co Inc. | openfda.manufacturer_name | |
| ndc | package | 42068-002-01 | openfda.package_ndc |
| ndc | package | 42068-002-02 | openfda.package_ndc |
| ndc | product | 42068-002 | openfda.product_ndc |
| ndc11 | package | 42068000201 | derived:openfda.package_ndc |
| ndc11 | package | 42068000202 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 40c02ca0-e79e-0920-e063-6394a90af7f0 | id | |
| spl set id | 7c242f6e-06a9-44cd-8aec-2d90ece44f44 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.