NDC Code | 69367-233-05 |
Package Description | 5 mL in 1 BOTTLE, DROPPER (69367-233-05) |
Product NDC | 69367-233 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Olopatadine Hydrochloride |
Non-Proprietary Name | Olopatadine Hydrochloride |
Dosage Form | SOLUTION/ DROPS |
Usage | OPHTHALMIC |
Start Marketing Date | 20190919 |
End Marketing Date | 20220502 |
Marketing Category Name | ANDA |
Application Number | ANDA203152 |
Manufacturer | Westminster Pharmaceuticals, LLC |
Substance Name | OLOPATADINE HYDROCHLORIDE |
Strength | 1 |
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] |