| NDC Code | 0185-0277-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0185-0277-01) |
|---|
| Product NDC | 0185-0277 |
|---|
| 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 | Sandoz Inc |
|---|
| Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 20; 25 |
|---|
| 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] |
|---|