| NDC Code | 71205-017-60 |
|---|
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-017-60) |
|---|
| Product NDC | 71205-017 |
|---|
| 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 | 20090917 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078906 |
|---|
| Manufacturer | Proficient Rx LP |
|---|
| Substance Name | VERAPAMIL HYDROCHLORIDE |
|---|
| Strength | 240 |
|---|
| 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] |
|---|