NDC Code | 68462-555-30 |
Package Description | 30 TABLET in 1 BOTTLE (68462-555-30) |
Product NDC | 68462-555 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Fosinopril Sodium And Hydrochlorothiazide |
Non-Proprietary Name | Fosinopril Sodium And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20090709 |
Marketing Category Name | ANDA |
Application Number | ANDA090228 |
Manufacturer | Glenmark Pharmaceuticals Inc., USA |
Substance Name | FOSINOPRIL SODIUM; 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] |