Product NDC: | 55154-6127 |
Proprietary Name: | Benicar |
Non Proprietary Name: | olmesartan medoxomil |
Active Ingredient(s): | 40 mg/1 & nbsp; olmesartan medoxomil |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-6127 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021286 |
Marketing Category: | NDA |
Start Marketing Date: | 20020425 |
Package NDC: | 55154-6127-8 |
Package Description: | 4590 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6127-8) |
NDC Code | 55154-6127-8 |
Proprietary Name | Benicar |
Package Description | 4590 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55154-6127-8) |
Product NDC | 55154-6127 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | olmesartan medoxomil |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20020425 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | OLMESARTAN MEDOXOMIL |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |