NDC Code | 37808-857-01 |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37808-857-01) / 5 mL in 1 BOTTLE, PLASTIC |
Product NDC | 37808-857 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Olopatadine Hydrochloride Ophthalmic Solution |
Non-Proprietary Name | Olopatadine Hydrochloride Ophthalmic |
Dosage Form | SOLUTION/ DROPS |
Usage | OPHTHALMIC |
Start Marketing Date | 20210315 |
Marketing Category Name | ANDA |
Application Number | ANDA209619 |
Manufacturer | HEB |
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] |