| NDC Code | 54569-6223-0 |
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| Package Description | 90 TABLET in 1 BOTTLE (54569-6223-0) |
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| Product NDC | 54569-6223 |
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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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| Marketing Category Name | ANDA |
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| Application Number | ANDA090528 |
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| Manufacturer | A-S Medication Solutions |
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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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