| NDC Code | 49349-702-20 |
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| Package Description | 100 TABLET in 1 BOTTLE (49349-702-20) |
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| Product NDC | 49349-702 |
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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 | 20150102 |
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| End Marketing Date | 20170330 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076194 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
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| Strength | 12.5; 10 |
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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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