NDC Code | 70518-0875-0 |
Package Description | 30 TABLET in 1 BLISTER PACK (70518-0875-0) |
Product NDC | 70518-0875 |
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 | 20171129 |
Marketing Category Name | ANDA |
Application Number | ANDA071251 |
Manufacturer | REMEDYREPACK INC. |
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] |