| NDC Code | 0185-0342-10 |
|---|
| Package Description | 1000 TABLET in 1 BOTTLE (0185-0342-10) |
|---|
| Product NDC | 0185-0342 |
|---|
| 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 | 20050928 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076961 |
|---|
| Manufacturer | Eon Labs, Inc. |
|---|
| 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 [Chemical/Ingredient] |
|---|