warnings
Warnings
Loratadine ODT
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
- Loratadine ODT
- Generic name
- LORATADINE
- Manufacturer
- Rugby Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f59f3400-da77-4eb7-be02-842071d87fae
- SPL ID
- e4fff55f-aace-428a-b474-e85cfd1fe6f5
- Version
- 2
- Effective date
- 2026-08-07
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:29
| 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 | 208477 | derived:openfda.application_number |
| application number | ANDA208477 | openfda.application_number | |
| brand name | Loratadine ODT | openfda.brand_name | |
| generic name | LORATADINE | openfda.generic_name | |
| manufacturer name | Rugby Laboratories | openfda.manufacturer_name | |
| ndc | package | 0536-1367-07 | openfda.package_ndc |
| ndc | product | 0536-1367 | openfda.product_ndc |
| ndc11 | package | 00536136707 | derived:openfda.package_ndc |
| rxcui | 311373 | openfda.rxcui | |
| spl id | e4fff55f-aace-428a-b474-e85cfd1fe6f5 | id | |
| spl set id | f59f3400-da77-4eb7-be02-842071d87fae | set_id | |
| unii | 7AJO3BO7QN | openfda.unii |
Warnings 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.