| NDC Code | 61786-765-19 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (61786-765-19) |
|---|
| Product NDC | 61786-765 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valsartan And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Valsartan And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160707 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091519 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | VALSARTAN; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 320; 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 [Chemical/Ingredient] |
|---|