| NDC Code | 65862-045-00 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (65862-045-00) |
|---|
| Product NDC | 65862-045 |
|---|
| 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 | 20060314 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077606 |
|---|
| Manufacturer | Aurobindo Pharma Limited |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
|---|
| Strength | 25; 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] |
|---|