NDC Code | 54868-4904-1 |
Package Description | 10 TABLET in 1 BOTTLE (54868-4904-1) |
Product NDC | 54868-4904 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Lotensin Hct |
Non-Proprietary Name | Benazepril Hydrochloride And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20030829 |
Marketing Category Name | NDA |
Application Number | NDA020033 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
Strength | 20; 12.5 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |