| NDC Code | 0781-1123-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (0781-1123-05) |
|---|
| Product NDC | 0781-1123 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Triamterene Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Triamterene And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19920430 |
|---|
| End Marketing Date | 20201130 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA073281 |
|---|
| Manufacturer | Sandoz Inc |
|---|
| Substance Name | TRIAMTERENE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 37.5; 25 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
|---|