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Quinapril HCl and Hydrochlorothiazide
Quinapril HCl and Hydrochlorothiazide - 43386-712-09 - (Quinapril HCl and Hydrochlorothiazide)
Drug Information of Quinapril HCl and Hydrochlorothiazide
| Product NDC: | 43386-712 |
| Proprietary Name: | Quinapril HCl and Hydrochlorothiazide |
| Non Proprietary Name: | Quinapril HCl and Hydrochlorothiazide |
| Active Ingredient(s): | 25; 20 mg/1; mg/1 & nbsp; Quinapril HCl and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Quinapril HCl and Hydrochlorothiazide
| Product NDC: | 43386-712 |
| Labeler Name: | GAVIS Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076374 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110715 |
Package Information of Quinapril HCl and Hydrochlorothiazide
| Package NDC: | 43386-712-09 |
| Package Description: | 90 TABLET in 1 BOTTLE (43386-712-09) |
NDC Information of Quinapril HCl and Hydrochlorothiazide
| NDC Code | 43386-712-09 |
| Proprietary Name | Quinapril HCl and Hydrochlorothiazide |
| Package Description | 90 TABLET in 1 BOTTLE (43386-712-09) |
| Product NDC | 43386-712 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Quinapril HCl and Hydrochlorothiazide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110715 |
| Marketing Category Name | ANDA |
| Labeler Name | GAVIS Pharmaceuticals, LLC |
| 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] |
