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
- ILMO Products Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7e0f2f4a-ac52-412c-97c6-0b4c44bdb5a5
- SPL ID
- 424c9d1a-8918-50f0-e063-6294a90ae5f7
- Version
- 15
- Effective date
- 2025-10-29
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:42
| 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 | ILMO Products Company | openfda.manufacturer_name | |
| ndc | package | 51486-002-08 | openfda.package_ndc |
| ndc | package | 51486-002-01 | openfda.package_ndc |
| ndc | package | 51486-002-07 | openfda.package_ndc |
| ndc | package | 51486-002-03 | openfda.package_ndc |
| ndc | package | 51486-002-02 | openfda.package_ndc |
| ndc | package | 51486-002-05 | openfda.package_ndc |
| ndc | package | 51486-002-09 | openfda.package_ndc |
| ndc | package | 51486-002-10 | openfda.package_ndc |
| ndc | package | 51486-002-06 | openfda.package_ndc |
| ndc | package | 51486-002-04 | openfda.package_ndc |
| ndc | product | 51486-002 | openfda.product_ndc |
| ndc11 | package | 51486000205 | derived:openfda.package_ndc |
| ndc11 | package | 51486000207 | derived:openfda.package_ndc |
| ndc11 | package | 51486000201 | derived:openfda.package_ndc |
| ndc11 | package | 51486000204 | derived:openfda.package_ndc |
| ndc11 | package | 51486000208 | derived:openfda.package_ndc |
| ndc11 | package | 51486000210 | derived:openfda.package_ndc |
| ndc11 | package | 51486000206 | derived:openfda.package_ndc |
| ndc11 | package | 51486000209 | derived:openfda.package_ndc |
| ndc11 | package | 51486000203 | derived:openfda.package_ndc |
| ndc11 | package | 51486000202 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 424c9d1a-8918-50f0-e063-6294a90ae5f7 | id | |
| spl set id | 7e0f2f4a-ac52-412c-97c6-0b4c44bdb5a5 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.