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
- SYOXSA, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 66b47ed5-82d0-44ba-a2aa-17db9b98ee22
- SPL ID
- 45c700db-8d21-cf27-e063-6394a90a8c4f
- Version
- 13
- Effective date
- 2025-12-12
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/5ab46f90f6b44e2aa9affb3cb9a1420d82b92a8f942c23fe463364760a659d66/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:08:17
| 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 | 205829 | derived:openfda.application_number |
| application number | NDA205829 | openfda.application_number | |
| brand name | Nitrogen | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | SYOXSA, Inc. | openfda.manufacturer_name | |
| ndc | package | 23647-002-06 | openfda.package_ndc |
| ndc | package | 23647-002-04 | openfda.package_ndc |
| ndc | package | 23647-002-02 | openfda.package_ndc |
| ndc | package | 23647-002-05 | openfda.package_ndc |
| ndc | package | 23647-002-03 | openfda.package_ndc |
| ndc | package | 23647-002-01 | openfda.package_ndc |
| ndc | package | 23647-002-07 | openfda.package_ndc |
| ndc | product | 23647-002 | openfda.product_ndc |
| ndc11 | package | 23647000207 | derived:openfda.package_ndc |
| ndc11 | package | 23647000206 | derived:openfda.package_ndc |
| ndc11 | package | 23647000202 | derived:openfda.package_ndc |
| ndc11 | package | 23647000201 | derived:openfda.package_ndc |
| ndc11 | package | 23647000205 | derived:openfda.package_ndc |
| ndc11 | package | 23647000204 | derived:openfda.package_ndc |
| ndc11 | package | 23647000203 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 45c700db-8d21-cf27-e063-6394a90a8c4f | id | |
| spl set id | 66b47ed5-82d0-44ba-a2aa-17db9b98ee22 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.