| NDC Code | 0781-5068-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (0781-5068-05) |
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| Product NDC | 0781-5068 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Triamterene Hydrochlorothiazide |
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| Non-Proprietary Name | Triamterene And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20170420 |
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| End Marketing Date | 20200930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA073281 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | TRIAMTERENE; HYDROCHLOROTHIAZIDE |
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| Strength | 37.5; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
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