| NDC Code | 51672-4045-3 |
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| Package Description | 1000 TABLET in 1 BOTTLE (51672-4045-3) |
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| Product NDC | 51672-4045 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Enalapril Maleate And Hydrochlorothiazide |
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| Non-Proprietary Name | Enalapril Maleate And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20010918 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075788 |
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| Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
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| Substance Name | ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
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| Strength | 5; 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 [CS] |
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