| NDC Code | 42292-017-20 |
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| Package Description | 100 BLISTER PACK in 1 CARTON (42292-017-20) / 1 TABLET in 1 BLISTER PACK (42292-017-01) |
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| Product NDC | 42292-017 |
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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 | 20170512 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA086513 |
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| Manufacturer | Mylan Institutional Inc. |
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| Substance Name | HYDROCHLOROTHIAZIDE; SPIRONOLACTONE |
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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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