| NDC Code | 58118-4745-0 |
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| Package Description | 1 TABLET, FILM COATED in 1 PACKAGE (58118-4745-0) |
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| Product NDC | 58118-4745 |
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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 | 20121203 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076688 |
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| Manufacturer | Clinical Solutions Wholesale |
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| Substance Name | BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
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| Strength | 20; 12.5 |
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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 [Chemical/Ingredient] |
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