| NDC Code | 68462-555-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (68462-555-01) |
|---|
| 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] |
|---|