Product NDC: | 35356-216 |
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: | 35356-216 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021286 |
Marketing Category: | NDA |
Start Marketing Date: | 20120222 |
Package NDC: | 35356-216-90 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-216-90) |
NDC Code | 35356-216-90 |
Proprietary Name | Benicar |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-216-90) |
Product NDC | 35356-216 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | olmesartan medoxomil |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120222 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | OLMESARTAN MEDOXOMIL |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |