PATADAY ONCE DAILY RELIEF is a Ophthalmic Solution in the Human Otc Drug category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is Olopatadine Hydrochloride.
| Product ID | 0065-0816_56a040cc-fda3-412d-8217-20d0e07deef3 |
| NDC | 0065-0816 |
| Product Type | Human Otc Drug |
| Proprietary Name | PATADAY ONCE DAILY RELIEF |
| Generic Name | Olopatadine Hydrochloride |
| Dosage Form | Solution |
| Route of Administration | OPHTHALMIC |
| Marketing Start Date | 2020-09-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA206276 |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | OLOPATADINE HYDROCHLORIDE |
| Active Ingredient Strength | 7 mg/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2021-01-04 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0065-0816 | PATADAY ONCE DAILY RELIEF | OLOPATADINE HYDROCHLORIDE |
| 0065-8150 | PATADAY ONCE DAILY RELIEF | OLOPATADINE HYDROCHLORIDE |
| 17478-105 | Olopatadine | Olopatadine Hydrochloride |
| 17478-305 | Olopatadine | Olopatadine Hydrochloride |
| 0093-7684 | Olopatadine Hydrochloride | Olopatadine Hydrochloride |
| 0363-0200 | OLOPATADINE HYDROCHLORIDE | OLOPATADINE HYDROCHLORIDE |
| 0363-8022 | OLOPATADINE HYDROCHLORIDE | OLOPATADINE HYDROCHLORIDE |
| 0378-8023 | Olopatadine Hydrochloride | Olopatadine Hydrochloride |
| 0065-0272 | PATADAY | olopatadine hydrochloride |
| 0065-4274 | PATADAY TWICE A DAY RELIEF | OLOPATADINE HYDROCHLORIDE |
| 0065-0332 | PATANASE | olopatadine hydrochloride |
| 0078-0834 | PATANASE | olopatadine hydrochloride |
| 0065-0271 | Patanol | olopatadine hydrochloride |
| 0065-4273 | Pazeo | olopatadine hydrochloride |