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BENICAR HCT
BENICAR HCT - 55154-6125-2 - (olmesartan medoxomil and hydrochlorothiazide)
Drug Information of BENICAR HCT
| Product NDC: | 55154-6125 |
| Proprietary Name: | BENICAR HCT |
| Non Proprietary Name: | olmesartan medoxomil and hydrochlorothiazide |
| Active Ingredient(s): | 12.5; 20 mg/1; mg/1 & nbsp; olmesartan medoxomil and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BENICAR HCT
| Product NDC: | 55154-6125 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021532 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030605 |
Package Information of BENICAR HCT
| Package NDC: | 55154-6125-2 |
| Package Description: | 4680 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6125-2) |
NDC Information of BENICAR HCT
| NDC Code | 55154-6125-2 |
| Proprietary Name | BENICAR HCT |
| Package Description | 4680 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6125-2) |
| Product NDC | 55154-6125 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | olmesartan medoxomil and hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030605 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL |
| Strength Number | 12.5; 20 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
