| NDC Code | 43386-712-03 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (43386-712-03) |
|---|
| Product NDC | 43386-712 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Quinapril Hcl And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Quinapril Hcl And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110715 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076374 |
|---|
| Manufacturer | Lupin 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 [CS] |
|---|