Nitrous Oxide
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
- Nitrous Oxide
- Generic name
- NITROUS OXIDE
- Manufacturer
- Lessors, Incorporated
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b18bf991-bc6e-4678-99c0-61d7cbdb171a
- SPL ID
- 410d77e3-f9bd-66e2-e063-6394a90a781d
- Version
- 18
- Effective date
- 2025-10-13
- Source export date
- 2026-11-06
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:02:51
| 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 | 209989 | derived:openfda.application_number |
| application number | NDA209989 | openfda.application_number | |
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Lessors, Incorporated | openfda.manufacturer_name | |
| ndc | package | 55404-002-07 | openfda.package_ndc |
| ndc | package | 55404-002-06 | openfda.package_ndc |
| ndc | package | 55404-002-02 | openfda.package_ndc |
| ndc | package | 55404-002-05 | openfda.package_ndc |
| ndc | package | 55404-002-03 | openfda.package_ndc |
| ndc | package | 55404-002-04 | openfda.package_ndc |
| ndc | package | 55404-002-01 | openfda.package_ndc |
| ndc | product | 55404-002 | openfda.product_ndc |
| ndc11 | package | 55404000205 | derived:openfda.package_ndc |
| ndc11 | package | 55404000204 | derived:openfda.package_ndc |
| ndc11 | package | 55404000201 | derived:openfda.package_ndc |
| ndc11 | package | 55404000202 | derived:openfda.package_ndc |
| ndc11 | package | 55404000206 | derived:openfda.package_ndc |
| ndc11 | package | 55404000203 | derived:openfda.package_ndc |
| ndc11 | package | 55404000207 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 410d77e3-f9bd-66e2-e063-6394a90a781d | id | |
| spl set id | b18bf991-bc6e-4678-99c0-61d7cbdb171a | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.