| NDC Code | 60505-0209-2 |
|---|
| Package Description | 1000 TABLET in 1 BOTTLE (60505-0209-2) |
|---|
| Product NDC | 60505-0209 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Enalapril Maleate And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Enalapril Maleate And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20070619 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076486 |
|---|
| Manufacturer | Apotex Corp. |
|---|
| Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 10; 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 [Chemical/Ingredient] |
|---|