| NDC Code | 0378-0544-93 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0544-93) |
|---|
| Product NDC | 0378-0544 |
|---|
| 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 | 20070226 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077093 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| 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 [Chemical/Ingredient] |
|---|