| NDC Code | 51991-836-75 |
|---|
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (51991-836-75) / 5 mL in 1 BOTTLE, DROPPER |
|---|
| Product NDC | 51991-836 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Epinastine Hydrochloride |
|---|
| Non-Proprietary Name | Epinastine Hydrochloride |
|---|
| Dosage Form | SOLUTION/ DROPS |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 20131105 |
|---|
| End Marketing Date | 20240930 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090870 |
|---|
| Manufacturer | Breckenridge Pharmaceutical, Inc. |
|---|
| Substance Name | EPINASTINE HYDROCHLORIDE |
|---|
| Strength | .5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Adrenergic Agonists [MoA], Adrenergic Receptor Agonist [EPC], Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Inhibitor [EPC] |
|---|