| NDC Code | 52125-567-02 |
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| Package Description | 30 TABLET, FILM COATED in 1 VIAL (52125-567-02) |
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| Product NDC | 52125-567 |
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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 | 20130708 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077157 |
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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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