| NDC Code | 60505-0263-3 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (60505-0263-3) |
|---|
| Product NDC | 60505-0263 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Benazepril Hydrochloride And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Benazepril Hydrochloride And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140821 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078794 |
|---|
| Manufacturer | Apotex Corp. |
|---|
| 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] |
|---|