NDC Code |
0378-0577-05 |
Proprietary Name |
Amiloride Hydrochloride and Hydrochlorothiazide |
Package Description |
500 TABLET in 1 BOTTLE, PLASTIC (0378-0577-05) |
Product NDC |
0378-0577 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
amiloride hydrochloride and hydrochlorothiazide |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20110907 |
Marketing Category Name |
ANDA |
Labeler Name |
Mylan Pharmaceuticals Inc. |
Substance Name |
AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
Strength Number |
5; 50 |
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] |