| NDC Code | 68462-554-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE (68462-554-10) |
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| Product NDC | 68462-554 |
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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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| Marketing Category Name | ANDA |
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| Application Number | ANDA090228 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | FOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE |
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| Strength | 10; 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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