Quinapril Hydrochloride and Hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Apotex Corp. The primary component is Quinapril Hydrochloride; Hydrochlorothiazide.
| Product ID | 60505-3411_2f57297f-2474-af8f-6a64-f6089889f4cb |
| NDC | 60505-3411 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Quinapril Hydrochloride and Hydrochlorothiazide |
| Generic Name | Quinapril Hydrochloride And Hydrochlorothiazide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2013-03-12 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA091524 |
| Labeler Name | Apotex Corp |
| 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 | 2019-12-31 |
| Marketing Start Date | 2013-03-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA091524 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-03-12 |
| Marketing End Date | 2020-06-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091524 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-03-12 |
| Marketing End Date | 2020-06-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091524 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-03-12 |
| Marketing End Date | 2020-06-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091524 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-03-12 |
| Marketing End Date | 2020-06-30 |
| Marketing Category | ANDA |
| Application Number | ANDA091524 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-03-12 |
| Marketing End Date | 2020-06-30 |
| Ingredient | Strength |
|---|---|
| QUINAPRIL HYDROCHLORIDE | 20 mg/1 |
| SPL SET ID: | ae34a8e0-5f82-4aa8-d71c-b7a3f720925c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 31722-374 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 31722-375 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 31722-376 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 59762-0220 | quinapril hydrochloride and hydrochlorothiazide | quinapril hydrochloride and hydrochlorothiazide |
| 59762-0222 | quinapril hydrochloride and hydrochlorothiazide | quinapril hydrochloride and hydrochlorothiazide |
| 59762-0223 | quinapril hydrochloride and hydrochlorothiazide | quinapril hydrochloride and hydrochlorothiazide |
| 60505-3409 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 60505-3410 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 60505-3411 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 63304-161 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 63304-162 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 63304-163 | Quinapril Hydrochloride and Hydrochlorothiazide | Quinapril Hydrochloride and Hydrochlorothiazide |
| 0071-0220 | ACCURETIC | quinapril hydrochloride and hydrochlorothiazide |
| 0071-0222 | ACCURETIC | quinapril hydrochloride and hydrochlorothiazide |
| 0071-0223 | ACCURETIC | quinapril hydrochloride and hydrochlorothiazide |