NDC Code | 0378-8023-35 |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0378-8023-35) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 0378-8023 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Olopatadine Hydrochloride |
Non-Proprietary Name | Olopatadine Hydrochloride |
Dosage Form | SOLUTION/ DROPS |
Usage | OPHTHALMIC |
Start Marketing Date | 20180912 |
End Marketing Date | 20211231 |
Marketing Category Name | ANDA |
Application Number | ANDA204392 |
Manufacturer | Mylan Pharmaceuticals Inc. |
Substance Name | OLOPATADINE HYDROCHLORIDE |
Strength | 1 |
Strength Unit | mg/mL |
Pharmacy Classes | Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] |