| NDC Code | 70518-0786-0 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0786-0) |
|---|
| Product NDC | 70518-0786 |
|---|
| 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 | 20171012 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091617 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 100; 25 |
|---|
| 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] |
|---|