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
- AGL Inhalation Therapy Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 08461574-4ad0-4749-a200-53abcad5b1ee
- SPL ID
- 4cc1bbf1-cb91-1798-e063-6294a90a46fb
- Version
- 13
- Effective date
- 2026-03-02
- Source export date
- 2026-10-27
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:16:24
| 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 | AGL Inhalation Therapy Co. | openfda.manufacturer_name | |
| ndc | package | 17575-006-13 | openfda.package_ndc |
| ndc | package | 17575-006-12 | openfda.package_ndc |
| ndc | package | 17575-006-18 | openfda.package_ndc |
| ndc | package | 17575-006-15 | openfda.package_ndc |
| ndc | package | 17575-006-11 | openfda.package_ndc |
| ndc | package | 17575-006-04 | openfda.package_ndc |
| ndc | package | 17575-006-14 | openfda.package_ndc |
| ndc | package | 17575-006-17 | openfda.package_ndc |
| ndc | package | 17575-006-07 | openfda.package_ndc |
| ndc | package | 17575-006-01 | openfda.package_ndc |
| ndc | package | 17575-006-03 | openfda.package_ndc |
| ndc | package | 17575-006-08 | openfda.package_ndc |
| ndc | package | 17575-006-16 | openfda.package_ndc |
| ndc | package | 17575-006-02 | openfda.package_ndc |
| ndc | package | 17575-006-05 | openfda.package_ndc |
| ndc | package | 17575-006-06 | openfda.package_ndc |
| ndc | package | 17575-006-10 | openfda.package_ndc |
| ndc | package | 17575-006-09 | openfda.package_ndc |
| ndc | product | 17575-006 | openfda.product_ndc |
| ndc11 | package | 17575000606 | derived:openfda.package_ndc |
| ndc11 | package | 17575000615 | derived:openfda.package_ndc |
| ndc11 | package | 17575000616 | derived:openfda.package_ndc |
| ndc11 | package | 17575000617 | derived:openfda.package_ndc |
| ndc11 | package | 17575000618 | derived:openfda.package_ndc |
| ndc11 | package | 17575000611 | derived:openfda.package_ndc |
| ndc11 | package | 17575000613 | derived:openfda.package_ndc |
| ndc11 | package | 17575000604 | derived:openfda.package_ndc |
| ndc11 | package | 17575000601 | derived:openfda.package_ndc |
| ndc11 | package | 17575000610 | derived:openfda.package_ndc |
| ndc11 | package | 17575000614 | derived:openfda.package_ndc |
| ndc11 | package | 17575000603 | derived:openfda.package_ndc |
| ndc11 | package | 17575000608 | derived:openfda.package_ndc |
| ndc11 | package | 17575000609 | derived:openfda.package_ndc |
| ndc11 | package | 17575000607 | derived:openfda.package_ndc |
| ndc11 | package | 17575000612 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.