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
- 2026-09-28
- 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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:54
| 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.