| NDC Code | 82868-054-30 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (82868-054-30) |
|---|
| Product NDC | 82868-054 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valsartan And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Valsartan And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240521 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203145 |
|---|
| Manufacturer | Northwind Pharmaceuticals, LLC |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; VALSARTAN |
|---|
| Strength | 25; 160 |
|---|
| 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] |
|---|