quinapril and hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Greenstone Llc. The primary component is Quinapril Hydrochloride; Hydrochlorothiazide.
| Product ID | 59762-5225_46a33cf7-f5c5-4afb-b464-27a36773fe52 |
| NDC | 59762-5225 |
| Product Type | Human Prescription Drug |
| Proprietary Name | quinapril and hydrochlorothiazide |
| Generic Name | Quinapril And Hydrochlorothiazide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-10-25 |
| Marketing Category | NDA AUTHORIZED GENERIC / |
| Application Number | NDA020125 |
| Labeler Name | Greenstone LLC |
| 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 |
| Marketing Start Date | 2021-10-25 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA020125 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-12-10 |
| Marketing End Date | 2019-12-10 |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 59762-5225 | quinapril and hydrochlorothiazide | quinapril and hydrochlorothiazide |
| 0071-3112 | ACCURETIC | quinapril and hydrochlorothiazide |
| 0071-5212 | ACCURETIC | quinapril and hydrochlorothiazide |