NDC 70518-1464
VERAPAMIL HYDROCHLORIDE
Verapamil Hydrochloride
VERAPAMIL HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Verapamil Hydrochloride.
Product ID | 70518-1464_7770a43f-b445-140b-e053-2991aa0a4816 |
NDC | 70518-1464 |
Product Type | Human Prescription Drug |
Proprietary Name | VERAPAMIL HYDROCHLORIDE |
Generic Name | Verapamil Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2018-10-04 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA071881 |
Labeler Name | REMEDYREPACK INC. |
Substance Name | VERAPAMIL HYDROCHLORIDE |
Active Ingredient Strength | 120 mg/1 |
Pharm Classes | P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |