| NDC Code | 68084-518-21 |
|---|
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-518-21) > 10 TABLET in 1 BLISTER PACK (68084-518-11) |
|---|
| Product NDC | 68084-518 |
|---|
| 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 | 20130612 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077912 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
|---|
| Strength | 12.5; 10 |
|---|
| 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] |
|---|