NITROGEN NF
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 NF
- Generic name
- NITROGEN
- Manufacturer
- Norco, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 1119f82c-0441-4c4f-8423-4518d0d1f060
- SPL ID
- 460169a7-56b6-ad4e-e063-6294a90ac25d
- Version
- 13
- Effective date
- 2025-12-15
- Source export date
- 2026-11-06
- 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/2026-11-06/3744b3ae389d13e8f30cade845ea29e0fc75bb043dcda980c2025693f0c10522/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 09:07:03
| 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 | 205805 | derived:openfda.application_number |
| application number | NDA205805 | openfda.application_number | |
| brand name | NITROGEN NF | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | Norco, Inc | openfda.manufacturer_name | |
| ndc | package | 42602-005-04 | openfda.package_ndc |
| ndc | package | 42602-005-05 | openfda.package_ndc |
| ndc | package | 42602-005-11 | openfda.package_ndc |
| ndc | package | 42602-005-02 | openfda.package_ndc |
| ndc | package | 42602-005-01 | openfda.package_ndc |
| ndc | package | 42602-005-08 | openfda.package_ndc |
| ndc | package | 42602-005-10 | openfda.package_ndc |
| ndc | package | 42602-005-06 | openfda.package_ndc |
| ndc | package | 42602-005-09 | openfda.package_ndc |
| ndc | package | 42602-005-03 | openfda.package_ndc |
| ndc | package | 42602-005-07 | openfda.package_ndc |
| ndc | product | 42602-005 | openfda.product_ndc |
| ndc11 | package | 42602000506 | derived:openfda.package_ndc |
| ndc11 | package | 42602000501 | derived:openfda.package_ndc |
| ndc11 | package | 42602000510 | derived:openfda.package_ndc |
| ndc11 | package | 42602000509 | derived:openfda.package_ndc |
| ndc11 | package | 42602000511 | derived:openfda.package_ndc |
| ndc11 | package | 42602000504 | derived:openfda.package_ndc |
| ndc11 | package | 42602000507 | derived:openfda.package_ndc |
| ndc11 | package | 42602000508 | derived:openfda.package_ndc |
| ndc11 | package | 42602000505 | derived:openfda.package_ndc |
| ndc11 | package | 42602000503 | derived:openfda.package_ndc |
| ndc11 | package | 42602000502 | derived:openfda.package_ndc |
| rxcui | 348987 | openfda.rxcui | |
| spl id | 460169a7-56b6-ad4e-e063-6294a90ac25d | id | |
| spl set id | 1119f82c-0441-4c4f-8423-4518d0d1f060 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.