| NDC Code | 59762-5014-1 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (59762-5014-1) |
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| Product NDC | 59762-5014 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19780101 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA012616 |
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| Manufacturer | Greenstone LLC |
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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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