| NDC Code | 53489-144-05 |
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| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (53489-144-05) |
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| Product NDC | 53489-144 |
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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 | 19870702 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089534 |
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| Manufacturer | Sun Pharmaceutical Industries, 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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