NDC 71335-0147
verapamil hydrochloride
Verapamil Hydrochloride
verapamil hydrochloride is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Verapamil Hydrochloride.
Product ID | 71335-0147_c7647f8c-87a2-4ec7-bedc-a3ca68f8f132 |
NDC | 71335-0147 |
Product Type | Human Prescription Drug |
Proprietary Name | verapamil hydrochloride |
Generic Name | Verapamil Hydrochloride |
Dosage Form | Tablet, Film Coated, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2009-09-17 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA078906 |
Labeler Name | Bryant Ranch Prepack |
Substance Name | VERAPAMIL HYDROCHLORIDE |
Active Ingredient Strength | 240 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 |