| NDC Code | 54569-6091-1 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (54569-6091-1) |
|---|
| Product NDC | 54569-6091 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lisinopril With Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20020708 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076265 |
|---|
| Manufacturer | A-S Medication Solutions |
|---|
| 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] |
|---|