| NDC Code | 60505-0264-1 |
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| Package Description | 100 TABLET in 1 BOTTLE (60505-0264-1) |
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| Product NDC | 60505-0264 |
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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 |
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| Usage | ORAL |
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| Start Marketing Date | 20140821 |
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| End Marketing Date | 20200531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078794 |
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| Manufacturer | Apotex Corp. |
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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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