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
- CEE-KAY SUPPLY, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 53f88c55-5c28-4a93-852b-894b0999e27d
- SPL ID
- 4bae4903-6d73-0bf3-e063-6394a90a14d6
- Version
- 22
- Effective date
- 2026-02-25
- 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 06:17:25
| 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 | 205766 | derived:openfda.application_number |
| application number | NDA205766 | openfda.application_number | |
| brand name | NITROGEN | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | CEE-KAY SUPPLY, INC. | openfda.manufacturer_name | |
| ndc | package | 10218-102-03 | openfda.package_ndc |
| ndc | package | 10218-102-01 | openfda.package_ndc |
| ndc | package | 10218-102-10 | openfda.package_ndc |
| ndc | package | 10218-102-08 | openfda.package_ndc |
| ndc | package | 10218-102-05 | openfda.package_ndc |
| ndc | package | 10218-102-06 | openfda.package_ndc |
| ndc | package | 10218-102-02 | openfda.package_ndc |
| ndc | package | 10218-102-11 | openfda.package_ndc |
| ndc | package | 10218-102-07 | openfda.package_ndc |
| ndc | package | 10218-102-09 | openfda.package_ndc |
| ndc | package | 10218-102-04 | openfda.package_ndc |
| ndc | product | 10218-102 | openfda.product_ndc |
| ndc11 | package | 10218010209 | derived:openfda.package_ndc |
| ndc11 | package | 10218010203 | derived:openfda.package_ndc |
| ndc11 | package | 10218010211 | derived:openfda.package_ndc |
| ndc11 | package | 10218010206 | derived:openfda.package_ndc |
| ndc11 | package | 10218010210 | derived:openfda.package_ndc |
| ndc11 | package | 10218010204 | derived:openfda.package_ndc |
| ndc11 | package | 10218010202 | derived:openfda.package_ndc |
| ndc11 | package | 10218010208 | derived:openfda.package_ndc |
| ndc11 | package | 10218010207 | derived:openfda.package_ndc |
| ndc11 | package | 10218010205 | derived:openfda.package_ndc |
| ndc11 | package | 10218010201 | derived:openfda.package_ndc |
| rxcui | 347021 | openfda.rxcui | |
| spl id | 4bae4903-6d73-0bf3-e063-6394a90a14d6 | id | |
| spl set id | 53f88c55-5c28-4a93-852b-894b0999e27d | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.