| NDC Code | 60505-3758-9 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (60505-3758-9) |
|---|
| Product NDC | 60505-3758 |
|---|
| 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 | 20121204 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202884 |
|---|
| Manufacturer | Apotex Corp. |
|---|
| Substance Name | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 16; 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 [Chemical/Ingredient] |
|---|