| NDC Code | 50268-794-15 |
|---|
| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-794-15) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-794-11) |
|---|
| Product NDC | 50268-794 |
|---|
| 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 | 20160801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078946 |
|---|
| Manufacturer | AvPAK |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; VALSARTAN |
|---|
| Strength | 25; 320 |
|---|
| 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] |
|---|