NDC Code | 68083-230-01 |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (68083-230-01) > 5 mL in 1 BOTTLE, PLASTIC |
Product NDC | 68083-230 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Olopatadine Hydrochloride |
Non-Proprietary Name | Olopatadine Hydrochloride Ophthalmic Solution Usp, 0.1% |
Dosage Form | SOLUTION/ DROPS |
Usage | OPHTHALMIC |
Start Marketing Date | 20170214 |
Marketing Category Name | ANDA |
Application Number | ANDA209619 |
Manufacturer | Gland Pharma Limited |
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] |