Amoxicillin 500 mg
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
- Amoxicillin 500 mg
- Generic name
- AMOXICILLIN
- Manufacturer
- Health Department, Oklahoma State
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f049551b-4708-eb13-e053-2a95a90afd1f
- SPL ID
- 45d711af-0b7c-998e-e063-6294a90a5ea4
- Version
- 3
- Effective date
- 2025-12-13
- Source export date
- 2026-10-27
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:06:15
| Harmonized routes |
|---|
| ORAL |
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 | ANDA | 065271 | derived:openfda.application_number |
| application number | ANDA065271 | openfda.application_number | |
| brand name | Amoxicillin 500 mg | openfda.brand_name | |
| generic name | AMOXICILLIN | openfda.generic_name | |
| manufacturer name | Health Department, Oklahoma State | openfda.manufacturer_name | |
| ndc | package | 83112-500-30 | openfda.package_ndc |
| ndc | package | 83112-500-21 | openfda.package_ndc |
| ndc | product | 83112-500 | openfda.product_ndc |
| ndc11 | package | 83112050030 | derived:openfda.package_ndc |
| ndc11 | package | 83112050021 | derived:openfda.package_ndc |
| rxcui | 308191 | openfda.rxcui | |
| spl id | 45d711af-0b7c-998e-e063-6294a90a5ea4 | id | |
| spl set id | f049551b-4708-eb13-e053-2a95a90afd1f | set_id | |
| unii | 804826J2HU | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.