| NDC Code | 68001-387-03 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (68001-387-03) |
|---|
| Product NDC | 68001-387 |
|---|
| 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 | 20190618 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA073449 |
|---|
| Manufacturer | BluePoint Laboratories |
|---|
| 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] |
|---|