NDC Code |
0591-2786-19 |
Proprietary Name |
Irbesartan and Hydrochlorothiazide |
Package Description |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-2786-19) |
Product NDC |
0591-2786 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
IRBESARTAN AND HYDROCHLOROTHIAZIDE |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20121022 |
Marketing Category Name |
ANDA |
Labeler Name |
Watson Laboratories, Inc. |
Substance Name |
HYDROCHLOROTHIAZIDE; IRBESARTAN |
Strength Number |
12.5; 300 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |