| NDC Code | 0603-4229-16 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0603-4229-16) |
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| Product NDC | 0603-4229 |
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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 | 20130215 |
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| End Marketing Date | 20170731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091617 |
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| Manufacturer | Qualitest Pharmaceuticals |
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| Substance Name | LOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE |
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| Strength | 100; 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 [Chemical/Ingredient] |
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