warnings
Warnings For external use only
OLOPATADINE HYDROCHLORIDE
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
- OLOPATADINE HYDROCHLORIDE
- Generic name
- OLOPATADINE HYDROCHLORIDE
- Manufacturer
- Amerisource Bergen
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 067baa0b-5c01-4908-92de-ad79c73d2c37
- SPL ID
- 1f56c080-a9b4-46ba-882b-3d3d92138ce6
- Version
- 5
- Effective date
- 2023-07-10
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:43:48
| 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 | 209995 | derived:openfda.application_number |
| application number | ANDA209995 | openfda.application_number | |
| brand name | OLOPATADINE HYDROCHLORIDE | openfda.brand_name | |
| generic name | OLOPATADINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Amerisource Bergen | openfda.manufacturer_name | |
| ndc | package | 46122-671-27 | openfda.package_ndc |
| ndc | product | 46122-671 | openfda.product_ndc |
| ndc11 | package | 46122067127 | derived:openfda.package_ndc |
| rxcui | 1111343 | openfda.rxcui | |
| spl id | 1f56c080-a9b4-46ba-882b-3d3d92138ce6 | id | |
| spl set id | 067baa0b-5c01-4908-92de-ad79c73d2c37 | set_id | |
| unii | 2XG66W44KF | 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.