Epinephrine Professional
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
- Epinephrine Professional
- Generic name
- EPINEPHRINE AND ISOPROPYL ALCOHOL
- Manufacturer
- Focus Health Group
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 8c502fcc-1b61-7d1f-e053-2a95a90adc46
- SPL ID
- 4a92cc7f-ec1f-e2d0-e063-6394a90aff25
- Version
- 7
- Effective date
- 2026-02-11
- Source export date
- 2026-10-27
- 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/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:58:10
| Harmonized routes |
|---|
| INTRAMUSCULAR, SUBCUTANEOUS |
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 | 204200 | derived:openfda.application_number |
| application number | NDA204200 | openfda.application_number | |
| brand name | Epinephrine Professional | openfda.brand_name | |
| generic name | EPINEPHRINE AND ISOPROPYL ALCOHOL | openfda.generic_name | |
| manufacturer name | Focus Health Group | openfda.manufacturer_name | |
| ndc | package | 68599-5804-1 | openfda.package_ndc |
| ndc | package | 42023-159-25 | openfda.package_ndc |
| ndc | package | 24357-011-13 | openfda.package_ndc |
| ndc | product | 24357-011 | openfda.product_ndc |
| ndc11 | package | 42023015925 | derived:openfda.package_ndc |
| ndc11 | package | 24357001113 | derived:openfda.package_ndc |
| ndc11 | package | 68599580401 | derived:openfda.package_ndc |
| rxcui | 1660016 | openfda.rxcui | |
| rxcui | 1660014 | openfda.rxcui | |
| rxcui | 797544 | openfda.rxcui | |
| spl id | 4a92cc7f-ec1f-e2d0-e063-6394a90aff25 | id | |
| spl set id | 8c502fcc-1b61-7d1f-e053-2a95a90adc46 | set_id |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.