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Benicar
Benicar - 51138-213-30 - (olmesartan medoxomil)
Drug Information of Benicar
| Product NDC: | 51138-213 |
| 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) |
Labeler Information of Benicar
| Product NDC: | 51138-213 |
| Labeler Name: | Med-Health Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021286 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120202 |
Package Information of Benicar
| Package NDC: | 51138-213-30 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-213-30) |
NDC Information of Benicar
| NDC Code | 51138-213-30 |
| Proprietary Name | Benicar |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-213-30) |
| Product NDC | 51138-213 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | olmesartan medoxomil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120202 |
| Marketing Category Name | NDA |
| Labeler Name | Med-Health Pharma, LLC |
| Substance Name | OLMESARTAN MEDOXOMIL |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
