| NDC Code | 68084-946-21 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-946-21) > 1 TABLET in 1 BLISTER PACK (68084-946-11) |
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| Product NDC | 68084-946 |
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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 | 20150331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089534 |
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| Manufacturer | American Health Packaging |
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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 [Chemical/Ingredient] |
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