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
- 5101bf55-cacf-42bf-8dd1-2a29e80ca6f1
- SPL ID
- bb8e6b6b-70fd-48b7-b43d-23180531dc9f
- Version
- 5
- Effective date
- 2022-07-01
- Source export date
- 2026-11-06
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:54:24
| 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 | 064067 | derived:openfda.application_number |
| application number | ANDA064067 | 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 | 63187-608-35 | openfda.package_ndc |
| ndc | product | 63187-608 | openfda.product_ndc |
| ndc11 | package | 63187060835 | derived:openfda.package_ndc |
| rxcui | 310149 | openfda.rxcui | |
| spl id | bb8e6b6b-70fd-48b7-b43d-23180531dc9f | id | |
| spl set id | 5101bf55-cacf-42bf-8dd1-2a29e80ca6f1 | 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.