NDC 70069-008
EPINASTINE HYDROCHLORIDE
Epinastine Hydrochloride
EPINASTINE HYDROCHLORIDE is a Ophthalmic Solution/ Drops in the Human Prescription Drug category.  It is labeled and distributed by Somerset Therapeutics, Llc. The primary component is Epinastine Hydrochloride.
| Product ID | 70069-008_775198aa-738b-4d22-813a-4c22e4ff750d | 
| NDC | 70069-008 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | EPINASTINE HYDROCHLORIDE | 
| Generic Name | Epinastine Hydrochloride | 
| Dosage Form | Solution/ Drops | 
| Route of Administration | OPHTHALMIC | 
| Marketing Start Date | 2016-09-14 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA090951 | 
| Labeler Name | Somerset Therapeutics, LLC | 
| Substance Name | EPINASTINE HYDROCHLORIDE | 
| Active Ingredient Strength | 1 mg/mL | 
| Pharm Classes | Adrenergic Agonists [MoA],Adrenergic Receptor Agonist [EPC],Decreased Histamine Release [PE],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Inhibitor [EPC] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2022-12-31 |