NDC Code | 50090-2974-0 |
Package Description | 30 TABLET in 1 BOTTLE (50090-2974-0) |
Product NDC | 50090-2974 |
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 | 20061004 |
Marketing Category Name | ANDA |
Application Number | ANDA077912 |
Manufacturer | A-S Medication Solutions |
Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
Strength | 25; 20 |
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] |