NDC Code | 62559-662-90 |
Package Description | 90 TABLET in 1 BOTTLE (62559-662-90) |
Product NDC | 62559-662 |
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 | 20180926 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA021093 |
Manufacturer | ANI Pharmaceuticals, Inc. |
Substance Name | CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE |
Strength | 32; 25 |
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] |