| NDC Code | 54458-921-05 |
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| Package Description | 360 TABLET in 1 CARTON (54458-921-05) |
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| Product NDC | 54458-921 |
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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 | 20101015 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077912 |
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| Manufacturer | International Laboratories, LLC |
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| Substance Name | LISINOPRIL; 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],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
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