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
- MEDICAL-TECHNICAL GASES, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d676898d-c455-44c6-83b7-d5f19d10264b
- SPL ID
- 44731ea9-3851-4cb2-e063-6294a90a6d0a
- Version
- 11
- Effective date
- 2025-11-25
- Source export date
- 2026-10-30
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/eb45a4bb6908a5d117668eac8da5ce490c753c3f9b68298758ef131307d1d264/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:18:40
| 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 | MEDICAL-TECHNICAL GASES, INC. | openfda.manufacturer_name | |
| ndc | package | 10736-017-06 | openfda.package_ndc |
| ndc | package | 10736-017-01 | openfda.package_ndc |
| ndc | package | 10736-017-05 | openfda.package_ndc |
| ndc | package | 10736-017-04 | openfda.package_ndc |
| ndc | package | 10736-017-03 | openfda.package_ndc |
| ndc | package | 10736-017-02 | openfda.package_ndc |
| ndc | product | 10736-017 | openfda.product_ndc |
| ndc11 | package | 10736001705 | derived:openfda.package_ndc |
| ndc11 | package | 10736001702 | derived:openfda.package_ndc |
| ndc11 | package | 10736001701 | derived:openfda.package_ndc |
| ndc11 | package | 10736001703 | derived:openfda.package_ndc |
| ndc11 | package | 10736001704 | derived:openfda.package_ndc |
| ndc11 | package | 10736001706 | derived:openfda.package_ndc |
| rxcui | 347046 | openfda.rxcui | |
| spl id | 44731ea9-3851-4cb2-e063-6294a90a6d0a | id | |
| spl set id | d676898d-c455-44c6-83b7-d5f19d10264b | set_id | |
| unii | K50XQU1029 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.