approval · primary record
OLOPATADINE HYDROCHLORIDE
FDA · NDA · 2025-04-15
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2025-04-15 |
| Brand | PATADAY ONCE DAILY RELIEF |
| Sponsor | ALCON LABS INC |
| Route | OPHTHALMIC |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:35:52.742Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:OLOPATADINE HYDROCHLORIDE:2025-04-15
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