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
- Wilson Products Compressed Gas Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 895f2818-db4b-4533-8b0b-780f8c556de8
- SPL ID
- c5017f89-8e38-4788-8301-615b338110a2
- Version
- 4
- Effective date
- 2024-10-29
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:41:00
| 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 | Wilson Products Compressed Gas Co. | openfda.manufacturer_name | |
| ndc | package | 51105-002-01 | openfda.package_ndc |
| ndc | package | 51105-002-02 | openfda.package_ndc |
| ndc | product | 51105-002 | openfda.product_ndc |
| ndc11 | package | 51105000202 | derived:openfda.package_ndc |
| ndc11 | package | 51105000201 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | c5017f89-8e38-4788-8301-615b338110a2 | id | |
| spl set id | 895f2818-db4b-4533-8b0b-780f8c556de8 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.