| NDC Code | 68788-9461-6 |
|---|
| Package Description | 60 TABLET in 1 BOTTLE (68788-9461-6) |
|---|
| Product NDC | 68788-9461 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160614 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078245 |
|---|
| Manufacturer | Preferred Pharmaceuticals, Inc. |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
|---|
| Strength | 25; 100 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
|---|