| NDC Code | 54569-0502-0 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (54569-0502-0) |
|---|
| Product NDC | 54569-0502 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Spironolactone And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Spironolactone And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19780101 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA012616 |
|---|
| Manufacturer | A-S Medication Solutions LLC |
|---|
| 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] |
|---|