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
- All Gas & Welding Supplies Co., Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f43540c0-741c-78c3-e053-2995a90aa2d4
- SPL ID
- 43e21a08-1c64-3aef-e063-6294a90ac8f7
- Version
- 4
- Effective date
- 2025-11-18
- Source export date
- 2026-10-30
- 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/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:58:36
| 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 | 205866 | derived:openfda.application_number |
| application number | NDA205866 | openfda.application_number | |
| brand name | Nitrogen | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | All Gas & Welding Supplies Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 56130-003-01 | openfda.package_ndc |
| ndc | package | 56130-003-02 | openfda.package_ndc |
| ndc | product | 56130-003 | openfda.product_ndc |
| ndc11 | package | 56130000302 | derived:openfda.package_ndc |
| ndc11 | package | 56130000301 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 43e21a08-1c64-3aef-e063-6294a90ac8f7 | id | |
| spl set id | f43540c0-741c-78c3-e053-2995a90aa2d4 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.