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
- Quality Air Products Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 044d220f-99fc-49ba-b4ad-18ff54d805f1
- SPL ID
- 458681a4-40a2-aeb4-e063-6294a90afa5c
- Version
- 18
- Effective date
- 2025-12-09
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:54:46
| 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 | 206009 | derived:openfda.application_number |
| application number | NDA206009 | openfda.application_number | |
| brand name | Nitrous Oxide | openfda.brand_name | |
| generic name | NITROUS OXIDE | openfda.generic_name | |
| manufacturer name | Quality Air Products Inc | openfda.manufacturer_name | |
| ndc | package | 63978-201-01 | openfda.package_ndc |
| ndc | package | 63978-201-03 | openfda.package_ndc |
| ndc | package | 63978-201-02 | openfda.package_ndc |
| ndc | package | 63978-201-04 | openfda.package_ndc |
| ndc | package | 63978-201-05 | openfda.package_ndc |
| ndc | product | 63978-201 | openfda.product_ndc |
| ndc11 | package | 63978020105 | derived:openfda.package_ndc |
| ndc11 | package | 63978020102 | derived:openfda.package_ndc |
| ndc11 | package | 63978020101 | derived:openfda.package_ndc |
| ndc11 | package | 63978020104 | derived:openfda.package_ndc |
| ndc11 | package | 63978020103 | derived:openfda.package_ndc |
| rxcui | 312022 | openfda.rxcui | |
| spl id | 458681a4-40a2-aeb4-e063-6294a90afa5c | id | |
| spl set id | 044d220f-99fc-49ba-b4ad-18ff54d805f1 | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.