QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Quinapril Hydrochloride; Hydrochlorothiazide.
| Product ID | 65862-163_23194091-fa77-4035-b9c1-3120faba7e7e |
| NDC | 65862-163 |
| Product Type | Human Prescription Drug |
| Proprietary Name | QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE |
| Generic Name | Quinapril Hydrochloride/hydrochlorothiazide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2007-08-24 |
| Marketing Category | ANDA / DRUG FOR FURTHER PROCESSING |
| Application Number | ANDA078450 |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | QUINAPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Active Ingredient Strength | 20 mg/1; mg/1 |
| Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |