Olopatadine is a Ophthalmic Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Akorn. The primary component is Olopatadine Hydrochloride.
Product ID | 17478-312_4df9962a-31a1-454d-9e4a-a86927409e5e |
NDC | 17478-312 |
Product Type | Human Otc Drug |
Proprietary Name | Olopatadine |
Generic Name | Olopatadine Hydrochloride |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2021-09-01 |
Marketing Category | ANDA / |
Application Number | ANDA204723 |
Labeler Name | Akorn |
Substance Name | OLOPATADINE HYDROCHLORIDE |
Active Ingredient Strength | 2 mg/mL |
Pharm Classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2021-09-01 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
17478-105 | Olopatadine | Olopatadine Hydrochloride |
17478-305 | Olopatadine | Olopatadine Hydrochloride |
50090-3489 | Olopatadine | Olopatadine |
50090-3552 | Olopatadine | Olopatadine |
60429-957 | Olopatadine | Olopatadine |
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 |
0065-0816 | PATADAY ONCE DAILY RELIEF | OLOPATADINE HYDROCHLORIDE |
0065-8150 | PATADAY ONCE DAILY RELIEF | 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 |