| NDC Code | 0781-5817-92 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (0781-5817-92) |
|---|
| Product NDC | 0781-5817 |
|---|
| 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 | 19950428 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA020387 |
|---|
| Manufacturer | Sandoz Inc. |
|---|
| Substance Name | LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 100; 12.5 |
|---|
| 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] |
|---|