| NDC Code | 68001-215-03 |
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| Package Description | 500 TABLET in 1 BOTTLE (68001-215-03) |
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| Product NDC | 68001-215 |
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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 | 20140226 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA072011 |
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| Manufacturer | BluePoint Laboratories |
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| Substance Name | TRIAMTERENE; HYDROCHLOROTHIAZIDE |
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| Strength | 75; 50 |
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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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