| NDC Code | 0378-0141-01 |
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| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0141-01) |
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| Product NDC | 0378-0141 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Spironolactone And Hydrochlorothiazide |
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| Non-Proprietary Name | Spironolactone And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20120726 |
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| End Marketing Date | 20200229 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA086513 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | SPIRONOLACTONE; HYDROCHLOROTHIAZIDE |
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| Strength | 25; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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