NDC Code | 71335-0870-1 |
Package Description | 30 TABLET in 1 BOTTLE (71335-0870-1) |
Product NDC | 71335-0870 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Enalapril Maleate And Hydrochlorothiazide |
Non-Proprietary Name | Enalapril Maleate And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20160331 |
Marketing Category Name | ANDA |
Application Number | ANDA075727 |
Manufacturer | Bryant Ranch Prepack |
Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
Strength | 10; 25 |
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 [CS] |