| NDC Code | 59762-0132-1 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59762-0132-1) |
|---|
| Product NDC | 59762-0132 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Trandolapril And Verapamil Hydrochloride |
|---|
| Proprietary Name Suffix | Er |
|---|
| Non-Proprietary Name | Trandolapril And Verapamil Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150225 |
|---|
| End Marketing Date | 20210528 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020591 |
|---|
| Manufacturer | Greenstone LLC |
|---|
| Substance Name | TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE |
|---|
| Strength | 2; 240 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA] |
|---|