| NDC Code | 68462-579-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68462-579-01) |
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| Product NDC | 68462-579 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Benazepril Hydrochloride And Hydrochlorothiazide |
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| Non-Proprietary Name | Benazepril 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 | 20040211 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076631 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
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| Strength | 20; 25 |
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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], Decreased Blood Pressure [PE], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
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