Product ID | 69097-828_4d3f7e7a-ed61-4df6-bc45-f38fb4117406 |
NDC | 69097-828 |
Product Type | Human Prescription Drug |
Proprietary Name | Quinapril and Hydrochlorothiazide 10/12.5 |
Generic Name | Quinapril And Hydrochlorothiazide 10/12.5 |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2016-07-20 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA201356 |
Labeler Name | Cipla USA Inc. |
Substance Name | QUINAPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
Active Ingredient Strength | 10 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 | 2023-12-31 |