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
- Indiana Oxygen Company Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- a116dc52-9522-4cc3-b745-0b0cc3e0d7dd
- SPL ID
- 3900254d-9785-4335-b041-9841d2aca5d2
- Version
- 13
- Effective date
- 2024-10-23
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:17
| 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 | 205767 | derived:openfda.application_number |
| application number | NDA205767 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Indiana Oxygen Company Inc | openfda.manufacturer_name | |
| ndc | package | 48546-0002-2 | openfda.package_ndc |
| ndc | package | 48546-0004-3 | openfda.package_ndc |
| ndc | package | 48546-0001-9 | openfda.package_ndc |
| ndc | package | 48546-0006-2 | openfda.package_ndc |
| ndc | package | 48546-0001-5 | openfda.package_ndc |
| ndc | package | 48546-0002-3 | openfda.package_ndc |
| ndc | package | 48546-0002-8 | openfda.package_ndc |
| ndc | package | 48546-0004-4 | openfda.package_ndc |
| ndc | package | 48546-0002-1 | openfda.package_ndc |
| ndc | package | 48546-0002-5 | openfda.package_ndc |
| ndc | package | 48546-0002-7 | openfda.package_ndc |
| ndc | package | 48546-0001-2 | openfda.package_ndc |
| ndc | package | 48546-0001-3 | openfda.package_ndc |
| ndc | package | 48546-0004-5 | openfda.package_ndc |
| ndc | package | 48546-0001-4 | openfda.package_ndc |
| ndc | package | 48546-0004-1 | openfda.package_ndc |
| ndc | package | 48546-0004-2 | openfda.package_ndc |
| ndc | package | 48546-0001-1 | openfda.package_ndc |
| ndc | package | 48546-0001-7 | openfda.package_ndc |
| ndc | package | 48546-0004-6 | openfda.package_ndc |
| ndc | package | 48546-0001-6 | openfda.package_ndc |
| ndc | package | 48546-0002-4 | openfda.package_ndc |
| ndc | package | 48546-0004-9 | openfda.package_ndc |
| ndc | package | 48546-0001-8 | openfda.package_ndc |
| ndc | package | 48546-0002-9 | openfda.package_ndc |
| ndc | package | 48546-0006-1 | openfda.package_ndc |
| ndc | package | 48546-0004-7 | openfda.package_ndc |
| ndc | package | 48546-0002-6 | openfda.package_ndc |
| ndc | package | 48546-0004-8 | openfda.package_ndc |
| ndc | product | 48546-0002 | openfda.product_ndc |
| ndc | product | 48546-0001 | openfda.product_ndc |
| ndc | product | 48546-0006 | openfda.product_ndc |
| ndc | product | 48546-0004 | openfda.product_ndc |
| ndc11 | package | 48546000105 | derived:openfda.package_ndc |
| ndc11 | package | 48546000208 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.