| NDC Code | 71335-0152-8 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8) |
|---|
| Product NDC | 71335-0152 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101006 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091629 |
|---|
| Manufacturer | Bryant Ranch Prepack |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
|---|
| Strength | 12.5; 50 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|