NDC Code | 68071-4687-3 |
Package Description | 30 TABLET in 1 BOTTLE (68071-4687-3) |
Product NDC | 68071-4687 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Triamterene And Hydrochlorothiazide |
Non-Proprietary Name | Triamterene And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 19930923 |
Marketing Category Name | ANDA |
Application Number | ANDA071851 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | HYDROCHLOROTHIAZIDE; TRIAMTERENE |
Strength | 50; 75 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |