| NDC Code | 59762-0222-1 |
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| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59762-0222-1) |
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| Product NDC | 59762-0222 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Quinapril Hydrochloride And Hydrochlorothiazide |
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| Non-Proprietary Name | Quinapril Hydrochloride And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19991228 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020125 |
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| Manufacturer | Greenstone LLC |
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| Substance Name | HYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE |
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| Strength | 12.5; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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