| NDC Code | 68462-205-30 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68462-205-30) |
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| Product NDC | 68462-205 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Moexipril Hydrochloride And Hydrochlorothiazide |
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| Non-Proprietary Name | Moexipril Hydrochloride And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20100318 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090718 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | MOEXIPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
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| Strength | 15; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
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