| NDC Code | 47781-137-36 |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (47781-137-36) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 47781-137 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Olopatadine Hydrochloride |
| Non-Proprietary Name | Olopatadine Hydrochloride Usp, 0.1% |
| Dosage Form | SOLUTION/ DROPS |
| Usage | OPHTHALMIC |
| Start Marketing Date | 20151208 |
| Marketing Category Name | ANDA |
| Application Number | ANDA204706 |
| Manufacturer | Alvogen 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] |