NDC Code | 54868-0699-2 |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-0699-2) |
Product NDC | 54868-0699 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Spironolactone And Hydrochlorothiazide |
Non-Proprietary Name | Spironolactone And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 19930526 |
Marketing Category Name | ANDA |
Application Number | ANDA086513 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | SPIRONOLACTONE; HYDROCHLOROTHIAZIDE |
Strength | 25; 25 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |