| NDC Code | 59762-0223-1 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0223-1) |
|---|
| Product NDC | 59762-0223 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Quinapril Hydrochloride And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Quinapril Hydrochloride And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19991228 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020125 |
|---|
| Manufacturer | Greenstone LLC |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
|---|
| 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] |
|---|