OXYGEN
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
- OXYGEN
- Generic name
- OXYGEN
- Manufacturer
- Clovis Equipment & Supply Company
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 55373dd8-3a52-439d-b4f0-649b237f57e8
- SPL ID
- 41d91937-460e-cefd-e063-6394a90af49d
- Version
- 8
- Effective date
- 2025-10-23
- Source export date
- 2026-09-28
- 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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:30
| 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 | 205889 | derived:openfda.application_number |
| application number | NDA205889 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Clovis Equipment & Supply Company | openfda.manufacturer_name | |
| ndc | package | 53730-001-07 | openfda.package_ndc |
| ndc | package | 53730-001-05 | openfda.package_ndc |
| ndc | package | 53730-001-03 | openfda.package_ndc |
| ndc | package | 53730-001-08 | openfda.package_ndc |
| ndc | package | 53730-001-01 | openfda.package_ndc |
| ndc | package | 53730-001-06 | openfda.package_ndc |
| ndc | package | 53730-001-02 | openfda.package_ndc |
| ndc | package | 53730-001-04 | openfda.package_ndc |
| ndc | product | 53730-001 | openfda.product_ndc |
| ndc11 | package | 53730000102 | derived:openfda.package_ndc |
| ndc11 | package | 53730000101 | derived:openfda.package_ndc |
| ndc11 | package | 53730000105 | derived:openfda.package_ndc |
| ndc11 | package | 53730000103 | derived:openfda.package_ndc |
| ndc11 | package | 53730000104 | derived:openfda.package_ndc |
| ndc11 | package | 53730000108 | derived:openfda.package_ndc |
| ndc11 | package | 53730000106 | derived:openfda.package_ndc |
| ndc11 | package | 53730000107 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 41d91937-460e-cefd-e063-6394a90af49d | id | |
| spl set id | 55373dd8-3a52-439d-b4f0-649b237f57e8 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.