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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
- Rising Pharma Holdings, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0988e6e2-59a9-47dc-9386-9e9ea877e6c1
- SPL ID
- d6814040-cbb9-4a23-aa29-e3d30bb97efc
- Version
- 2
- Effective date
- 2025-04-04
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:02
| 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 | 204620 | derived:openfda.application_number |
| application number | ANDA204620 | openfda.application_number | |
| brand name | olopatadine hydrochloride | openfda.brand_name | |
| generic name | OLOPATADINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Rising Pharma Holdings, Inc. | openfda.manufacturer_name | |
| ndc | package | 16571-861-25 | openfda.package_ndc |
| ndc | product | 16571-861 | openfda.product_ndc |
| ndc11 | package | 16571086125 | derived:openfda.package_ndc |
| rxcui | 1111343 | openfda.rxcui | |
| spl id | d6814040-cbb9-4a23-aa29-e3d30bb97efc | id | |
| spl set id | 0988e6e2-59a9-47dc-9386-9e9ea877e6c1 | 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.