| NDC Code | 68084-926-21 |
|---|
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-926-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-926-11) |
|---|
| Product NDC | 68084-926 |
|---|
| 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 | 20160622 |
|---|
| End Marketing Date | 20180131 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091519 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | VALSARTAN; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 80; 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 [Chemical/Ingredient] |
|---|