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 | 60505-3410_2f57297f-2474-af8f-6a64-f6089889f4cb |
NDC | 60505-3410 |
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 |
Marketing Start Date | 2013-03-12 |
Marketing End Date | 2019-11-30 |
Marketing Category | ANDA |
Application Number | ANDA091524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-12 |
Marketing End Date | 2019-11-30 |
Marketing Category | ANDA |
Application Number | ANDA091524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-12 |
Marketing End Date | 2019-11-30 |
Marketing Category | ANDA |
Application Number | ANDA091524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-12 |
Marketing End Date | 2019-11-30 |
Marketing Category | ANDA |
Application Number | ANDA091524 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-03-12 |
Marketing End Date | 2019-11-30 |
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 |