NDC Code | 51655-959-52 |
Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-959-52) |
Product NDC | 51655-959 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Verapamil Hydrochloride |
Non-Proprietary Name | Verapamil Hydrochloride |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20230131 |
Marketing Category Name | ANDA |
Application Number | ANDA090700 |
Manufacturer | Northwind Pharmaceuticals, LLC |
Substance Name | VERAPAMIL HYDROCHLORIDE |
Strength | 180 |
Strength Unit | mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA] |