| NDC Code | 52125-473-19 |
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| Package Description | 90 TABLET in 1 BOTTLE (52125-473-19) |
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| Product NDC | 52125-473 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
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| Non-Proprietary Name | Losartan Potassium And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20130205 |
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| End Marketing Date | 20171230 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090528 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
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| Strength | 12.5; 50 |
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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 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
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