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Quinapril Hydrochloride/Hydrochlorothiazide
Quinapril Hydrochloride/Hydrochlorothiazide - 65862-162-30 - (Quinapril Hydrochloride/Hydrochlorothiazide)
Drug Information of Quinapril Hydrochloride/Hydrochlorothiazide
| Product NDC: | 65862-162 |
| Proprietary Name: | Quinapril Hydrochloride/Hydrochlorothiazide |
| Non Proprietary Name: | Quinapril Hydrochloride/Hydrochlorothiazide |
| Active Ingredient(s): | 12.5; 20 mg/1; mg/1 & nbsp; Quinapril Hydrochloride/Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Quinapril Hydrochloride/Hydrochlorothiazide
| Product NDC: | 65862-162 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078450 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070824 |
Package Information of Quinapril Hydrochloride/Hydrochlorothiazide
| Package NDC: | 65862-162-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (65862-162-30) |
NDC Information of Quinapril Hydrochloride/Hydrochlorothiazide
| NDC Code | 65862-162-30 |
| Proprietary Name | Quinapril Hydrochloride/Hydrochlorothiazide |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (65862-162-30) |
| Product NDC | 65862-162 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Quinapril Hydrochloride/Hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070824 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
| Strength Number | 12.5; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
