NDC Code | 49349-600-02 |
Package Description | 30 TABLET in 1 BLISTER PACK (49349-600-02) |
Product NDC | 49349-600 |
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 | 20111102 |
Marketing Category Name | ANDA |
Application Number | ANDA073449 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | TRIAMTERENE; HYDROCHLOROTHIAZIDE |
Strength | 37.5; 25 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |