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
- Westair Gases & Equipment, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 0268620b-4e8b-4b62-a768-688b477e0171
- SPL ID
- 4487ca09-1ab2-1181-e063-6394a90a4d46
- Version
- 17
- Effective date
- 2025-11-26
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:38:17
| 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 | Westair Gases & Equipment, Inc. | openfda.manufacturer_name | |
| ndc | package | 53440-002-07 | openfda.package_ndc |
| ndc | package | 53440-002-08 | openfda.package_ndc |
| ndc | package | 53440-002-20 | openfda.package_ndc |
| ndc | package | 53440-002-06 | openfda.package_ndc |
| ndc | package | 53440-002-10 | openfda.package_ndc |
| ndc | package | 53440-002-09 | openfda.package_ndc |
| ndc | package | 53440-002-21 | openfda.package_ndc |
| ndc | package | 53440-002-19 | openfda.package_ndc |
| ndc | package | 53440-002-17 | openfda.package_ndc |
| ndc | package | 53440-002-13 | openfda.package_ndc |
| ndc | package | 53440-002-12 | openfda.package_ndc |
| ndc | package | 53440-002-15 | openfda.package_ndc |
| ndc | package | 53440-002-18 | openfda.package_ndc |
| ndc | package | 53440-002-04 | openfda.package_ndc |
| ndc | package | 53440-002-16 | openfda.package_ndc |
| ndc | package | 53440-002-14 | openfda.package_ndc |
| ndc | package | 53440-002-11 | openfda.package_ndc |
| ndc | package | 53440-002-02 | openfda.package_ndc |
| ndc | package | 53440-002-01 | openfda.package_ndc |
| ndc | package | 53440-002-22 | openfda.package_ndc |
| ndc | package | 53440-002-03 | openfda.package_ndc |
| ndc | package | 53440-002-05 | openfda.package_ndc |
| ndc | product | 53440-002 | openfda.product_ndc |
| ndc11 | package | 53440000206 | derived:openfda.package_ndc |
| ndc11 | package | 53440000201 | derived:openfda.package_ndc |
| ndc11 | package | 53440000211 | derived:openfda.package_ndc |
| ndc11 | package | 53440000203 | derived:openfda.package_ndc |
| ndc11 | package | 53440000204 | derived:openfda.package_ndc |
| ndc11 | package | 53440000205 | derived:openfda.package_ndc |
| ndc11 | package | 53440000207 | derived:openfda.package_ndc |
| ndc11 | package | 53440000202 | derived:openfda.package_ndc |
| ndc11 | package | 53440000221 | derived:openfda.package_ndc |
| ndc11 | package | 53440000209 | derived:openfda.package_ndc |
| ndc11 | package | 53440000212 | derived:openfda.package_ndc |
| ndc11 | package | 53440000220 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.