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
- AGP LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8e922dd4-c6ea-4ef6-9e26-35c599e8135b
- SPL ID
- 42ccd2bb-cbba-64b4-e063-6294a90a6d5d
- Version
- 11
- Effective date
- 2025-11-04
- Source export date
- 2026-10-30
- 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/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:49:51
| 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 | 205839 | derived:openfda.application_number |
| application number | NDA205839 | openfda.application_number | |
| brand name | NITROGEN | openfda.brand_name | |
| generic name | NITROGEN | openfda.generic_name | |
| manufacturer name | AGP LLC | openfda.manufacturer_name | |
| ndc | package | 22557-002-02 | openfda.package_ndc |
| ndc | package | 22557-002-01 | openfda.package_ndc |
| ndc | product | 22557-002 | openfda.product_ndc |
| ndc11 | package | 22557000201 | derived:openfda.package_ndc |
| ndc11 | package | 22557000202 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 42ccd2bb-cbba-64b4-e063-6294a90a6d5d | id | |
| spl set id | 8e922dd4-c6ea-4ef6-9e26-35c599e8135b | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.