| NDC Code | 0087-2876-31 | 
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			| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0087-2876-31) | 
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			| Product NDC | 0087-2876 | 
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			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
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			| Proprietary Name | Avalide | 
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			| Non-Proprietary Name | Irbesartan And Hydrochlorothiazide | 
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			| Dosage Form | TABLET, FILM COATED | 
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			| Usage | ORAL | 
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			| Start Marketing Date | 20110224 | 
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			| End Marketing Date | 20151130 | 
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			| Marketing Category Name | NDA | 
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			| Application Number | NDA020758 | 
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			| Manufacturer | Bristol-Myers Squibb Company | 
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			| Substance Name | IRBESARTAN; HYDROCHLOROTHIAZIDE | 
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			| Strength | 300; 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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