| NDC Code | 71335-0862-1 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (71335-0862-1) |
|---|
| Product NDC | 71335-0862 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20030304 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076194 |
|---|
| Manufacturer | Bryant Ranch Prepack |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
|---|
| Strength | 12.5; 20 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|