| NDC Code | 0054-0126-22 |
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| Package Description | 90 TABLET in 1 BOTTLE (0054-0126-22) |
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| Product NDC | 0054-0126 |
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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 | 20101006 |
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| End Marketing Date | 20190705 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077732 |
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| Manufacturer | West-Ward Pharmaceuticals Corp. |
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| Substance Name | LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE |
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| Strength | 50; 12.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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