| NDC Code | 23155-061-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (23155-061-05) |
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| Product NDC | 23155-061 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fosinopril Sodium And Hydrochlorothiazide |
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| Non-Proprietary Name | Fosinopril Sodium And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20111115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079025 |
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| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
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| Substance Name | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
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| Strength | 20; 12.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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