| NDC Code | 0555-0483-05 |
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| Package Description | 1000 TABLET in 1 BOTTLE (0555-0483-05) |
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| Product NDC | 0555-0483 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amiloride Hydrochloride And Hydrochlorothiazide |
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| Non-Proprietary Name | Amiloride Hydrochloride And Hydrochlorothiazide |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19891201 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA071111 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
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| Strength | 5; 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], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
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