NDC Code | 49349-074-20 |
Package Description | 100 TABLET in 1 VIAL (49349-074-20) |
Product NDC | 49349-074 |
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 | 20130821 |
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 | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC] |