FdaApplication
NDA 206276
Identifiers
- fda_app_no: NDA206276
Properties
| Property | Value |
|---|---|
| applicant_name | ALCON LABORATORIES INC |
| application_type | NDA |
| approval_date | 2015-01-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PATADAY ONCE DAILY RELIEF | OLOPATADINE HYDROCHLORIDE | EQ 0.7% BASE | SOLUTION/DROPS;OPHTHALMIC |
1 product