NDC Code |
68788-9850-3 |
Proprietary Name |
Benazepril Hydrochloride and Hydrochlorothiazide |
Package Description |
30 TABLET, FILM COATED in 1 BOTTLE (68788-9850-3) |
Product NDC |
68788-9850 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Benazepril Hydrochloride and Hydrochlorothiazide |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20120312 |
Marketing Category Name |
ANDA |
Labeler Name |
Preferred Pharmaceuticals, Inc |
Substance Name |
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
Strength Number |
20; 25 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |