| NDC Code | 68084-946-25 |
|---|
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-946-25) > 1 TABLET in 1 BLISTER PACK (68084-946-95) |
|---|
| Product NDC | 68084-946 |
|---|
| 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 | 20150331 |
|---|
| End Marketing Date | 20180228 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA089534 |
|---|
| Manufacturer | American Health Packaging |
|---|
| 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] |
|---|