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
- MAVERICK OXYGEN & RESPIRATORY EQUIPMENT, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9aa214de-957c-7abc-e053-2995a90acd83
- SPL ID
- 43e498bc-4241-9167-e063-6394a90a45e6
- Version
- 7
- Effective date
- 2025-11-18
- 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/2026-11-06/7dfa569f2d8f065241260fd9a4886d0ef0a3120fd6ee31d6d07c234e689e8c91/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:21:53
| 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 | MAVERICK OXYGEN & RESPIRATORY EQUIPMENT, LLC | openfda.manufacturer_name | |
| ndc | package | 67477-002-03 | openfda.package_ndc |
| ndc | package | 67477-002-01 | openfda.package_ndc |
| ndc | package | 67477-002-02 | openfda.package_ndc |
| ndc | product | 67477-002 | openfda.product_ndc |
| ndc11 | package | 67477000203 | derived:openfda.package_ndc |
| ndc11 | package | 67477000202 | derived:openfda.package_ndc |
| ndc11 | package | 67477000201 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 43e498bc-4241-9167-e063-6394a90a45e6 | id | |
| spl set id | 9aa214de-957c-7abc-e053-2995a90acd83 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.