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quinapril hydrochloride and hydrochlorothiazide
quinapril hydrochloride and hydrochlorothiazide - 59762-0223-1 - (QUINAPRIL HYDROCHLORIDE and HYDROCHLOROTHIAZIDE)
Drug Information of quinapril hydrochloride and hydrochlorothiazide
| Product NDC: | 59762-0223 |
| 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: | 59762-0223 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020125 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19991228 |
Package Information of quinapril hydrochloride and hydrochlorothiazide
| Package NDC: | 59762-0223-1 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0223-1) |
NDC Information of quinapril hydrochloride and hydrochlorothiazide
| NDC Code | 59762-0223-1 |
| Proprietary Name | quinapril hydrochloride and hydrochlorothiazide |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0223-1) |
| Product NDC | 59762-0223 |
| 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 | 19991228 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone 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] |
