| NDC Code | 68462-207-10 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-207-10) |
|---|
| Product NDC | 68462-207 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Moexipril Hydrochloride And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Moexipril Hydrochloride And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100318 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090718 |
|---|
| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
|---|
| Substance Name | MOEXIPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 7.5; 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] |
|---|