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 |