| NDC Code | 0093-7239-56 |
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| Package Description | 30 TABLET in 1 BOTTLE (0093-7239-56) |
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| Product NDC | 0093-7239 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Irbesartan And Hydrochlorothiazide |
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| Non-Proprietary Name | Irbesartan And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20120330 |
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| End Marketing Date | 20140228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077369 |
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| Manufacturer | Teva Pharmaceuticals USA Inc |
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| Substance Name | HYDROCHLOROTHIAZIDE; IRBESARTAN |
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| Strength | 12.5; 300 |
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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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