| NDC Code | 63629-2680-2 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (63629-2680-2) |
|---|
| Product NDC | 63629-2680 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Benazepril Hydrochloride And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Benazepril Hydrochloride And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20040211 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076631 |
|---|
| Manufacturer | Bryant Ranch Prepack |
|---|
| Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 20; 12.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|