warnings
WARNINGS
Loratadine
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
- Generic name
- LORATADINE
- Manufacturer
- Bryant Ranch Prepack
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7f97595b-9df7-4834-82f0-5e4ce329c118
- SPL ID
- 99fa3280-671d-46b4-8b66-94b9171c9ad7
- Version
- 1
- Effective date
- 2025-01-21
- Source export date
- 2026-10-12
- 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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:46:20
| 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 | 211718 | derived:openfda.application_number |
| application number | ANDA211718 | openfda.application_number | |
| brand name | Loratadine | openfda.brand_name | |
| generic name | LORATADINE | openfda.generic_name | |
| manufacturer name | Bryant Ranch Prepack | openfda.manufacturer_name | |
| ndc | package | 71335-2551-4 | openfda.package_ndc |
| ndc | package | 71335-2551-1 | openfda.package_ndc |
| ndc | package | 71335-2551-5 | openfda.package_ndc |
| ndc | package | 71335-2551-2 | openfda.package_ndc |
| ndc | package | 71335-2551-7 | openfda.package_ndc |
| ndc | package | 71335-2551-6 | openfda.package_ndc |
| ndc | package | 71335-2551-9 | openfda.package_ndc |
| ndc | package | 71335-2551-8 | openfda.package_ndc |
| ndc | package | 71335-2551-3 | openfda.package_ndc |
| ndc | product | 71335-2551 | openfda.product_ndc |
| ndc11 | package | 71335255108 | derived:openfda.package_ndc |
| ndc11 | package | 71335255105 | derived:openfda.package_ndc |
| ndc11 | package | 71335255103 | derived:openfda.package_ndc |
| ndc11 | package | 71335255101 | derived:openfda.package_ndc |
| ndc11 | package | 71335255107 | derived:openfda.package_ndc |
| ndc11 | package | 71335255109 | derived:openfda.package_ndc |
| ndc11 | package | 71335255104 | derived:openfda.package_ndc |
| ndc11 | package | 71335255102 | derived:openfda.package_ndc |
| ndc11 | package | 71335255106 | derived:openfda.package_ndc |
| rxcui | 311372 | openfda.rxcui | |
| spl id | 99fa3280-671d-46b4-8b66-94b9171c9ad7 | id | |
| spl set id | 7f97595b-9df7-4834-82f0-5e4ce329c118 | 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.