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
- Greene Respiratory Services, Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ecfdb289-b885-469b-8c60-c676be1df6ce
- SPL ID
- 9a514418-616a-4fdb-a594-766d910728b8
- Version
- 9
- Effective date
- 2025-11-25
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:03:10
| 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 | 205840 | derived:openfda.application_number |
| application number | NDA205840 | openfda.application_number | |
| brand name | OXYGEN | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Greene Respiratory Services, Inc | openfda.manufacturer_name | |
| ndc | package | 64140-101-03 | openfda.package_ndc |
| ndc | package | 64140-101-07 | openfda.package_ndc |
| ndc | package | 64140-101-01 | openfda.package_ndc |
| ndc | package | 64140-101-06 | openfda.package_ndc |
| ndc | package | 64140-101-08 | openfda.package_ndc |
| ndc | package | 64140-101-05 | openfda.package_ndc |
| ndc | package | 64140-101-02 | openfda.package_ndc |
| ndc | package | 64140-101-04 | openfda.package_ndc |
| ndc | product | 64140-101 | openfda.product_ndc |
| ndc11 | package | 64140010102 | derived:openfda.package_ndc |
| ndc11 | package | 64140010105 | derived:openfda.package_ndc |
| ndc11 | package | 64140010106 | derived:openfda.package_ndc |
| ndc11 | package | 64140010107 | derived:openfda.package_ndc |
| ndc11 | package | 64140010103 | derived:openfda.package_ndc |
| ndc11 | package | 64140010104 | derived:openfda.package_ndc |
| ndc11 | package | 64140010101 | derived:openfda.package_ndc |
| ndc11 | package | 64140010108 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 9a514418-616a-4fdb-a594-766d910728b8 | id | |
| spl set id | ecfdb289-b885-469b-8c60-c676be1df6ce | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.