warnings
Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
| Harmonized routes |
|---|
| ORAL |
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 | 210722 | derived:openfda.application_number |
| application number | ANDA210722 | openfda.application_number | |
| brand name | Loratadine | openfda.brand_name | |
| generic name | LORATADINE | openfda.generic_name | |
| manufacturer name | Advanced Rx LLC | openfda.manufacturer_name | |
| ndc | package | 80513-711-01 | openfda.package_ndc |
| ndc | package | 80513-711-03 | openfda.package_ndc |
| ndc | product | 80513-711 | openfda.product_ndc |
| ndc11 | package | 80513071101 | derived:openfda.package_ndc |
| ndc11 | package | 80513071103 | derived:openfda.package_ndc |
| rxcui | 311372 | openfda.rxcui | |
| spl id | 2efad4c4-593e-fa4d-e063-6294a90a0ebc | id | |
| spl set id | e96b4671-82dc-4cc6-a8bf-ef6f1efd8a7d | set_id | |
| unii | 7AJO3BO7QN | openfda.unii |
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.