| NDC Code | 68084-727-25 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-727-25) > 1 TABLET in 1 BLISTER PACK (68084-727-95) |
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| Product NDC | 68084-727 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Lisinopril And Hydrochlorothiazide |
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| Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20140501 |
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| End Marketing Date | 20180930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077912 |
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| Manufacturer | American Health Packaging |
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| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
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| Strength | 12.5; 20 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
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