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
- Asclemed USA, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- bccdb8f3-b5f5-4f07-8ddb-8811d5c1b73c
- SPL ID
- d9ae93e7-f4a8-1df3-e053-2a95a90ae5b1
- Version
- 1
- Effective date
- 2022-03-07
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:43:35
| 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 | Asclemed USA, Inc. | openfda.manufacturer_name | |
| ndc | package | 76420-212-30 | openfda.package_ndc |
| ndc | product | 76420-212 | openfda.product_ndc |
| ndc11 | package | 76420021230 | derived:openfda.package_ndc |
| rxcui | 310149 | openfda.rxcui | |
| spl id | d9ae93e7-f4a8-1df3-e053-2a95a90ae5b1 | id | |
| spl set id | bccdb8f3-b5f5-4f07-8ddb-8811d5c1b73c | 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.