| NDC Code | 70677-0122-1 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (70677-0122-1) / 2.5 mL in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 70677-0122 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Olopatadine Hydrochloride Ophthalmic Solution |
|---|
| Proprietary Name Suffix | Once Daily Relief |
|---|
| Non-Proprietary Name | Olopatadine Hydrochloride Ophthalmic |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20210315 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209752 |
|---|
| Manufacturer | Strategic Sourcing Specialists, LLC |
|---|
| Substance Name | OLOPATADINE HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| 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] |
|---|