| NDC Code | 68382-195-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (68382-195-01) |
|---|
| Product NDC | 68382-195 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Candesartan Cilexetil And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Candesartan Cilexetil And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180414 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203466 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 32; 12.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|