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Quinapril Hydrochloride and Hydrochlorothiazide
Quinapril Hydrochloride and Hydrochlorothiazide - 0378-0544-77 - (quinapril hydrochloride and hydrochlorothiazide)
Drug Information of Quinapril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 0378-0544 |
| Proprietary Name: | Quinapril Hydrochloride and Hydrochlorothiazide |
| Non Proprietary Name: | quinapril hydrochloride and hydrochlorothiazide |
| Active Ingredient(s): | 25; 20 mg/1; mg/1 & nbsp; quinapril hydrochloride and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Quinapril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 0378-0544 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077093 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121018 |
Package Information of Quinapril Hydrochloride and Hydrochlorothiazide
| Package NDC: | 0378-0544-77 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0544-77) |
NDC Information of Quinapril Hydrochloride and Hydrochlorothiazide
| NDC Code | 0378-0544-77 |
| Proprietary Name | Quinapril Hydrochloride and Hydrochlorothiazide |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0544-77) |
| Product NDC | 0378-0544 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | quinapril hydrochloride and hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121018 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
| Strength Number | 25; 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] |
