NDC Code |
21695-788-90 |
Proprietary Name |
HYZAAR |
Package Description |
90 TABLET, FILM COATED in 1 BOTTLE (21695-788-90) |
Product NDC |
21695-788 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
losartan potassium and hydrochlorothiazide |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
19950428 |
Marketing Category Name |
NDA |
Labeler Name |
Rebel Distributors Corp |
Substance Name |
HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
Strength Number |
25; 100 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |