NDC Code | 0172-5034-60 |
Package Description | 100 TABLET in 1 BOTTLE (0172-5034-60) |
Product NDC | 0172-5034 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Lisinopril And Hydrochlorothiazide |
Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20020701 |
Marketing Category Name | ANDA |
Application Number | ANDA075776 |
Manufacturer | Teva Pharmaceuticals USA, Inc. |
Substance Name | LISINOPRIL; HYDROCHLOROTHIAZIDE |
Strength | 20; 12.5 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |