| NDC Code |
68788-9850-9 |
| Proprietary Name |
Benazepril Hydrochloride and Hydrochlorothiazide |
| Package Description |
90 TABLET, FILM COATED in 1 BOTTLE (68788-9850-9) |
| 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] |