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
- Welders Supply Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- dde64850-2e2b-446e-9484-fc71c9a5d051
- SPL ID
- 47bb63cc-c050-d5e6-e063-6394a90a8078
- Version
- 22
- Effective date
- 2026-01-06
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:56
| 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 | Welders Supply Company | openfda.manufacturer_name | |
| ndc | package | 11999-002-01 | openfda.package_ndc |
| ndc | package | 11999-002-02 | openfda.package_ndc |
| ndc | product | 11999-002 | openfda.product_ndc |
| ndc11 | package | 11999000201 | derived:openfda.package_ndc |
| ndc11 | package | 11999000202 | derived:openfda.package_ndc |
| rxcui | 311998 | openfda.rxcui | |
| spl id | 47bb63cc-c050-d5e6-e063-6394a90a8078 | id | |
| spl set id | dde64850-2e2b-446e-9484-fc71c9a5d051 | set_id | |
| unii | N762921K75 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.