Benicar HCT is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Daiichi Sankyo, Inc.. The primary component is Olmesartan Medoxomil; Hydrochlorothiazide.
| Product ID | 65597-106_35032343-9c44-494e-a5a2-9aaf05381750 |
| NDC | 65597-106 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Benicar HCT |
| Generic Name | Olmesartan Medoxomil-hydrochlorothiazide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-06-05 |
| Marketing Category | NDA / NDA |
| Application Number | NDA021532 |
| Labeler Name | Daiichi Sankyo, Inc. |
| Substance Name | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
| Active Ingredient Strength | 40 mg/1; mg/1 |
| Pharm Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2003-07-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA021532 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-07-30 |
| Marketing Category | NDA |
| Application Number | NDA021532 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-07-30 |
| Marketing Category | NDA |
| Application Number | NDA021532 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2003-07-30 |
| Marketing Category | NDA |
| Application Number | NDA021532 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-07-30 |
| Marketing Category | NDA |
| Application Number | NDA021532 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-06-05 |
| Marketing End Date | 2012-10-09 |
| Ingredient | Strength |
|---|---|
| OLMESARTAN MEDOXOMIL | 40 mg/1 |
| SPL SET ID: | 6bbc032a-3cc4-4b1d-8124-1784214a2821 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0713-0863 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 0713-0864 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 0713-0865 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 50090-1083 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 55289-443 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 65597-105 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 65597-106 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 65597-107 | Benicar HCT | olmesartan medoxomil-hydrochlorothiazide |
| 50090-4329 | Olmesartan Medoxomil and Hydrochlorothiazide | olmesartan medoxomil-hydrochlorothiazide |
| 57664-758 | Olmesartan Medoxomil and Hydrochlorothiazide | olmesartan medoxomil-hydrochlorothiazide |
| 57664-759 | Olmesartan Medoxomil and Hydrochlorothiazide | olmesartan medoxomil-hydrochlorothiazide |
| 57664-760 | Olmesartan Medoxomil and Hydrochlorothiazide | olmesartan medoxomil-hydrochlorothiazide |
| 71335-0203 | Olmesartan Medoxomil and Hydrochlorothiazide | olmesartan medoxomil-hydrochlorothiazide |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BENICAR HCT 78323613 2928799 Live/Registered |
DAIICHI SANKYO COMPANY, LIMITED 2003-11-05 |
![]() BENICAR HCT 78308053 not registered Dead/Abandoned |
SANKYO COMPANY LIMITED 2003-10-01 |
![]() BENICAR HCT 78138481 2867773 Live/Registered |
DAIICHI SANKYO COMPANY, LIMITED 2002-06-25 |