Benicar - 51138-212-30 - (olmesartan medoxomil)

Alphabetical Index


Drug Information of Benicar

Product NDC: 51138-212
Proprietary Name: Benicar
Non Proprietary Name: olmesartan medoxomil
Active Ingredient(s): 20    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: 51138-212
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: 51138-212-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-212-30)

NDC Information of Benicar

NDC Code 51138-212-30
Proprietary Name Benicar
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51138-212-30)
Product NDC 51138-212
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 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

Complete Information of Benicar


General Information