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
- Roberts Oxygen Company, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 273511c2-2b84-4373-a0e5-3961eb19af8c
- SPL ID
- 43ceab71-8cc8-700c-e063-6294a90a3728
- Version
- 11
- Effective date
- 2025-11-17
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:26:28
| 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 | 205850 | derived:openfda.application_number |
| application number | NDA205850 | openfda.application_number | |
| brand name | Nitrogen | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | Roberts Oxygen Company, Inc | openfda.manufacturer_name | |
| ndc | package | 46123-003-03 | openfda.package_ndc |
| ndc | package | 46123-003-07 | openfda.package_ndc |
| ndc | package | 46123-003-05 | openfda.package_ndc |
| ndc | package | 46123-003-06 | openfda.package_ndc |
| ndc | package | 46123-003-02 | openfda.package_ndc |
| ndc | package | 46123-003-01 | openfda.package_ndc |
| ndc | package | 46123-003-04 | openfda.package_ndc |
| ndc | product | 46123-003 | openfda.product_ndc |
| ndc11 | package | 46123000304 | derived:openfda.package_ndc |
| ndc11 | package | 46123000303 | derived:openfda.package_ndc |
| ndc11 | package | 46123000302 | derived:openfda.package_ndc |
| ndc11 | package | 46123000305 | derived:openfda.package_ndc |
| ndc11 | package | 46123000301 | derived:openfda.package_ndc |
| ndc11 | package | 46123000306 | derived:openfda.package_ndc |
| ndc11 | package | 46123000307 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 43ceab71-8cc8-700c-e063-6294a90a3728 | id | |
| spl set id | 273511c2-2b84-4373-a0e5-3961eb19af8c | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.