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
- Air Liquide Large Industries U.S. LP
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f49fbee2-8a80-477a-969b-f891ee601dc3
- SPL ID
- a796c976-3dc3-4706-bfb8-d05fbe405975
- Version
- 21
- Effective date
- 2025-01-16
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:40:37
| 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 | 205738 | derived:openfda.application_number |
| application number | NDA205738 | openfda.application_number | |
| brand name | NITROGEN | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | Air Liquide Large Industries U.S. LP | openfda.manufacturer_name | |
| ndc | package | 11853-023-60 | openfda.package_ndc |
| ndc | package | 11853-023-61 | openfda.package_ndc |
| ndc | product | 11853-023 | openfda.product_ndc |
| ndc11 | package | 11853002360 | derived:openfda.package_ndc |
| ndc11 | package | 11853002361 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | a796c976-3dc3-4706-bfb8-d05fbe405975 | id | |
| spl set id | f49fbee2-8a80-477a-969b-f891ee601dc3 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.