NDC Code |
53808-0804-1 |
Proprietary Name |
Triamterene and Hydrochlorothiazide |
Package Description |
30 TABLET in 1 BLISTER PACK (53808-0804-1) |
Product NDC |
53808-0804 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
TRIAMTERENE AND HYDROCHLOROTHIAZIDE |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20090701 |
Marketing Category Name |
ANDA |
Labeler Name |
State of Florida DOH Central Pharmacy |
Substance Name |
HYDROCHLOROTHIAZIDE; TRIAMTERENE |
Strength Number |
50; 75 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |