Oxygen Compressed U.S.P
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 Compressed U.S.P
- Generic name
- OXYGEN
- Manufacturer
- Apria Healthcare LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 105a5557-c1af-42b1-859e-76cc1e83d9aa
- SPL ID
- 83452e77-1e11-4c72-bf20-def519a42cc1
- Version
- 24
- Effective date
- 2026-06-25
- Source export date
- 2026-10-30
- 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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:44:22
| 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 |
|---|---|---|---|
| brand name | Oxygen Compressed U.S.P | openfda.brand_name | |
| brand name | Oxygen Refrigerated Liquid U.S.P | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Apria Healthcare LLC | openfda.manufacturer_name | |
| ndc | package | 51319-073-01 | openfda.package_ndc |
| ndc | package | 51319-073-11 | openfda.package_ndc |
| ndc | package | 51319-073-04 | openfda.package_ndc |
| ndc | package | 51319-073-07 | openfda.package_ndc |
| ndc | package | 51319-073-13 | openfda.package_ndc |
| ndc | package | 51319-072-01 | openfda.package_ndc |
| ndc | package | 51319-073-02 | openfda.package_ndc |
| ndc | package | 51319-072-02 | openfda.package_ndc |
| ndc | package | 51319-073-10 | openfda.package_ndc |
| ndc | package | 51319-072-05 | openfda.package_ndc |
| ndc | package | 51319-073-03 | openfda.package_ndc |
| ndc | package | 51319-073-06 | openfda.package_ndc |
| ndc | package | 51319-073-09 | openfda.package_ndc |
| ndc | package | 51319-072-06 | openfda.package_ndc |
| ndc | package | 51319-073-08 | openfda.package_ndc |
| ndc | package | 51319-073-05 | openfda.package_ndc |
| ndc | package | 51319-072-04 | openfda.package_ndc |
| ndc | package | 51319-072-03 | openfda.package_ndc |
| ndc | package | 51319-073-12 | openfda.package_ndc |
| ndc | product | 51319-072 | openfda.product_ndc |
| ndc | product | 51319-073 | openfda.product_ndc |
| ndc11 | package | 51319007313 | derived:openfda.package_ndc |
| ndc11 | package | 51319007201 | derived:openfda.package_ndc |
| ndc11 | package | 51319007301 | derived:openfda.package_ndc |
| ndc11 | package | 51319007312 | derived:openfda.package_ndc |
| ndc11 | package | 51319007311 | derived:openfda.package_ndc |
| ndc11 | package | 51319007205 | derived:openfda.package_ndc |
| ndc11 | package | 51319007203 | derived:openfda.package_ndc |
| ndc11 | package | 51319007305 | derived:openfda.package_ndc |
| ndc11 | package | 51319007310 | derived:openfda.package_ndc |
| ndc11 | package | 51319007309 | derived:openfda.package_ndc |
| ndc11 | package | 51319007204 | derived:openfda.package_ndc |
| ndc11 | package | 51319007304 | derived:openfda.package_ndc |
| ndc11 | package | 51319007306 | derived:openfda.package_ndc |
| ndc11 | package | 51319007202 | derived:openfda.package_ndc |
| ndc11 | package | 51319007206 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.