NDC Code | 65597-105-90 |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (65597-105-90) |
Product NDC | 65597-105 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Benicar Hct |
Non-Proprietary Name | Olmesartan Medoxomil-hydrochlorothiazide |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20030605 |
End Marketing Date | 20230930 |
Marketing Category Name | NDA |
Application Number | NDA021532 |
Manufacturer | Daiichi Sankyo, Inc. |
Substance Name | HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL |
Strength | 12.5; 20 |
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] |