| NDC Code | 68071-5085-5 |
|---|
| Package Description | 5 mL in 1 BOTTLE (68071-5085-5) |
|---|
| Product NDC | 68071-5085 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Olopatadine Hydrochloride |
|---|
| Non-Proprietary Name | Olopatadine Hydrochloride |
|---|
| Dosage Form | SOLUTION/ DROPS |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20160629 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206306 |
|---|
| Manufacturer | NuCare Pharmaceuticals,Inc. |
|---|
| Substance Name | OLOPATADINE HYDROCHLORIDE |
|---|
| Strength | 1.11 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Inhibitor [EPC] |
|---|