| NDC Code | 0574-0135-01 |
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| Package Description | 100 TABLET, COATED in 1 BOTTLE (0574-0135-01) |
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| Product NDC | 0574-0135 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Moexipril Hydrochloride And Hydrochlorothiazide |
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| Non-Proprietary Name | Moexipril Hydrochloride And Hydrochlorothiazide |
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| Dosage Form | TABLET, COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20090701 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090096 |
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| Manufacturer | Paddock Laboratories, Inc. |
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| Substance Name | HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
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| Strength | 25; 15 |
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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 [Chemical/Ingredient] |
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