| NDC Code | 71335-0356-2 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (71335-0356-2) |
|---|
| Product NDC | 71335-0356 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Triamterene And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Triamterene And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090921 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA071251 |
|---|
| Manufacturer | Bryant Ranch Prepack |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; TRIAMTERENE |
|---|
| Strength | 25; 37.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|