adverse reactions
ADVERSE REACTIONS: The most frequently reported adverse reactions are minor ocular irritations, redness, and hypersensitivity reactions.
Erythromycin
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
- Erythromycin
- Generic name
- ERYTHROMYCIN
- Manufacturer
- Proficient Rx LP
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 62896bec-669e-4f20-a1e4-4f99afd35d32
- SPL ID
- 4d6257b3-af7e-4c8a-bd1a-3b7906dbd981
- Version
- 4
- Effective date
- 2022-04-01
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:46:50
| Harmonized routes |
|---|
| OPHTHALMIC |
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 | 064030 | derived:openfda.application_number |
| application number | ANDA064030 | openfda.application_number | |
| brand name | Erythromycin | openfda.brand_name | |
| generic name | ERYTHROMYCIN | openfda.generic_name | |
| manufacturer name | Proficient Rx LP | openfda.manufacturer_name | |
| ndc | package | 63187-267-35 | openfda.package_ndc |
| ndc | product | 63187-267 | openfda.product_ndc |
| ndc11 | package | 63187026735 | derived:openfda.package_ndc |
| rxcui | 310149 | openfda.rxcui | |
| spl id | 4d6257b3-af7e-4c8a-bd1a-3b7906dbd981 | id | |
| spl set id | 62896bec-669e-4f20-a1e4-4f99afd35d32 | set_id | |
| unii | 63937KV33D | openfda.unii |
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.