| NDC Code | 61314-272-25 |
|---|
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (61314-272-25) > 2.5 mL in 1 BOTTLE, DROPPER |
|---|
| Product NDC | 61314-272 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Olopatadine Hydrochloride |
|---|
| Non-Proprietary Name | Olopatadine Hydrochloride |
|---|
| Dosage Form | SOLUTION/ DROPS |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20070215 |
|---|
| End Marketing Date | 20220930 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA021545 |
|---|
| Manufacturer | Sandoz Inc |
|---|
| Substance Name | OLOPATADINE HYDROCHLORIDE |
|---|
| Strength | 2 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Inhibitor [EPC] |
|---|