| NDC Code | 54569-3869-1 |
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| Package Description | 30 TABLET in 1 BOTTLE (54569-3869-1) |
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| Product NDC | 54569-3869 |
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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 | A-S Medication Solutions |
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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],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
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