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
- Minneapolis Oxygen Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c3fdbc5c-da70-4cbd-bdee-eddb4d852b26
- SPL ID
- 44eb832f-4438-0da1-e063-6394a90ae833
- Version
- 16
- Effective date
- 2025-12-01
- Source export date
- 2026-10-30
- 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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:28:04
| 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 | Minneapolis Oxygen Company | openfda.manufacturer_name | |
| ndc | package | 55147-002-02 | openfda.package_ndc |
| ndc | package | 55147-002-06 | openfda.package_ndc |
| ndc | package | 55147-002-09 | openfda.package_ndc |
| ndc | package | 55147-002-08 | openfda.package_ndc |
| ndc | package | 55147-002-04 | openfda.package_ndc |
| ndc | package | 55147-002-01 | openfda.package_ndc |
| ndc | package | 55147-002-03 | openfda.package_ndc |
| ndc | package | 55147-002-11 | openfda.package_ndc |
| ndc | package | 55147-002-12 | openfda.package_ndc |
| ndc | package | 55147-002-05 | openfda.package_ndc |
| ndc | package | 55147-002-10 | openfda.package_ndc |
| ndc | package | 55147-002-07 | openfda.package_ndc |
| ndc | product | 55147-002 | openfda.product_ndc |
| ndc11 | package | 55147000204 | derived:openfda.package_ndc |
| ndc11 | package | 55147000201 | derived:openfda.package_ndc |
| ndc11 | package | 55147000206 | derived:openfda.package_ndc |
| ndc11 | package | 55147000211 | derived:openfda.package_ndc |
| ndc11 | package | 55147000209 | derived:openfda.package_ndc |
| ndc11 | package | 55147000208 | derived:openfda.package_ndc |
| ndc11 | package | 55147000210 | derived:openfda.package_ndc |
| ndc11 | package | 55147000205 | derived:openfda.package_ndc |
| ndc11 | package | 55147000212 | derived:openfda.package_ndc |
| ndc11 | package | 55147000203 | derived:openfda.package_ndc |
| ndc11 | package | 55147000202 | derived:openfda.package_ndc |
| ndc11 | package | 55147000207 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 44eb832f-4438-0da1-e063-6394a90ae833 | id | |
| spl set id | c3fdbc5c-da70-4cbd-bdee-eddb4d852b26 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.