| NDC Code | 0093-7369-10 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (0093-7369-10) |
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| Product NDC | 0093-7369 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20100406 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077157 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
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| Strength | 12.5; 100 |
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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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