# PATADAY ONCE DAILY RELIEF
> **NDA206276** · New Drug Application · Sponsor: ALCON LABS INC · Approved 2015-01-30
## Drug
- **FDA Application Number:** NDA206276
- **Application type:** New Drug Application
- **Brand name:** PATADAY ONCE DAILY RELIEF
- **Generic name:** OLOPATADINE HYDROCHLORIDE
- **Active ingredients:** OLOPATADINE HYDROCHLORIDE
- **Dosage form:** SOLUTION/DROPS
- **Route:** OPHTHALMIC
- **Marketing status:** Over-the-counter
- **Sponsor:** ALCON LABS INC
- **Manufacturer:** Alcon Laboratories, Inc.
- **First approval:** 2015-01-30
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=206276)
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