| NDC Code | 59762-5251-1 |
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| Package Description | 30 TABLET in 1 BOTTLE (59762-5251-1) |
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| Product NDC | 59762-5251 |
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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 | 20090709 |
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| End Marketing Date | 20141130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079245 |
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| Manufacturer | Greenstone LLC |
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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 [Chemical/Ingredient] |
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