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
- HARTMAN BROTHERS, INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b8a4f8fa-2c11-4ee4-850d-d1ee80fb0000
- SPL ID
- 41edeb0c-4d63-d4fb-e063-6294a90aec6c
- Version
- 14
- Effective date
- 2025-10-24
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:26:19
| 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 | 205712 | derived:openfda.application_number |
| application number | NDA205712 | openfda.application_number | |
| brand name | Oxygen | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | HARTMAN BROTHERS, INC. | openfda.manufacturer_name | |
| ndc | package | 49204-001-19 | openfda.package_ndc |
| ndc | package | 49204-001-20 | openfda.package_ndc |
| ndc | package | 49204-001-13 | openfda.package_ndc |
| ndc | package | 49204-001-09 | openfda.package_ndc |
| ndc | package | 49204-001-05 | openfda.package_ndc |
| ndc | package | 49204-001-15 | openfda.package_ndc |
| ndc | package | 49204-001-06 | openfda.package_ndc |
| ndc | package | 49204-001-08 | openfda.package_ndc |
| ndc | package | 49204-001-17 | openfda.package_ndc |
| ndc | package | 49204-001-14 | openfda.package_ndc |
| ndc | package | 49204-001-16 | openfda.package_ndc |
| ndc | package | 49204-001-10 | openfda.package_ndc |
| ndc | package | 49204-001-11 | openfda.package_ndc |
| ndc | package | 49204-001-01 | openfda.package_ndc |
| ndc | package | 49204-001-18 | openfda.package_ndc |
| ndc | package | 49204-001-03 | openfda.package_ndc |
| ndc | package | 49204-001-07 | openfda.package_ndc |
| ndc | package | 49204-001-02 | openfda.package_ndc |
| ndc | package | 49204-001-04 | openfda.package_ndc |
| ndc | package | 49204-001-12 | openfda.package_ndc |
| ndc | product | 49204-001 | openfda.product_ndc |
| ndc11 | package | 49204000117 | derived:openfda.package_ndc |
| ndc11 | package | 49204000101 | derived:openfda.package_ndc |
| ndc11 | package | 49204000118 | derived:openfda.package_ndc |
| ndc11 | package | 49204000113 | derived:openfda.package_ndc |
| ndc11 | package | 49204000112 | derived:openfda.package_ndc |
| ndc11 | package | 49204000104 | derived:openfda.package_ndc |
| ndc11 | package | 49204000114 | derived:openfda.package_ndc |
| ndc11 | package | 49204000109 | derived:openfda.package_ndc |
| ndc11 | package | 49204000116 | derived:openfda.package_ndc |
| ndc11 | package | 49204000115 | derived:openfda.package_ndc |
| ndc11 | package | 49204000105 | derived:openfda.package_ndc |
| ndc11 | package | 49204000103 | derived:openfda.package_ndc |
| ndc11 | package | 49204000110 | derived:openfda.package_ndc |
| ndc11 | package | 49204000119 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.