| NDC Code | 61786-998-19 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (61786-998-19) |
|---|
| Product NDC | 61786-998 |
|---|
| 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 | 20161116 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077912 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
|---|
| Strength | 12.5; 20 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
|---|