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
- Medical-Technical Gases, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- eb3cfc21-907d-ae13-e053-2a95a90a15c6
- SPL ID
- 44731f6c-743c-2fc9-e063-6294a90ad084
- Version
- 4
- Effective date
- 2025-11-25
- Source export date
- 2026-09-28
- 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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:54
| 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 | Medical-Technical Gases, Inc. | openfda.manufacturer_name | |
| ndc | package | 10736-203-09 | openfda.package_ndc |
| ndc | package | 10736-203-01 | openfda.package_ndc |
| ndc | package | 10736-203-07 | openfda.package_ndc |
| ndc | package | 10736-203-02 | openfda.package_ndc |
| ndc | package | 10736-203-05 | openfda.package_ndc |
| ndc | package | 10736-203-03 | openfda.package_ndc |
| ndc | package | 10736-203-08 | openfda.package_ndc |
| ndc | package | 10736-203-04 | openfda.package_ndc |
| ndc | package | 10736-203-06 | openfda.package_ndc |
| ndc | product | 10736-203 | openfda.product_ndc |
| ndc11 | package | 10736020308 | derived:openfda.package_ndc |
| ndc11 | package | 10736020306 | derived:openfda.package_ndc |
| ndc11 | package | 10736020303 | derived:openfda.package_ndc |
| ndc11 | package | 10736020302 | derived:openfda.package_ndc |
| ndc11 | package | 10736020307 | derived:openfda.package_ndc |
| ndc11 | package | 10736020301 | derived:openfda.package_ndc |
| ndc11 | package | 10736020304 | derived:openfda.package_ndc |
| ndc11 | package | 10736020305 | derived:openfda.package_ndc |
| ndc11 | package | 10736020309 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 44731f6c-743c-2fc9-e063-6294a90ad084 | id | |
| spl set id | eb3cfc21-907d-ae13-e053-2a95a90a15c6 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.