NDC Code | 0065-8150-07 |
Package Description | 3 BOTTLE, PLASTIC in 1 CARTON (0065-8150-07) / 2.5 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0065-8150 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Pataday Once Daily Relief |
Non-Proprietary Name | Olopatadine Hydrochloride |
Dosage Form | SOLUTION |
Usage | OPHTHALMIC |
Start Marketing Date | 20200228 |
Marketing Category Name | NDA |
Application Number | NDA021545 |
Manufacturer | Alcon Laboratories, Inc. |
Substance Name | OLOPATADINE HYDROCHLORIDE |
Strength | 2 |
Strength Unit | mg/mL |
Pharmacy Classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC] |