Benicar - 63629-3390-1 - (olmesartan medoxomil)

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Drug Information of Benicar

Product NDC: 63629-3390
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: 63629-3390
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021286
Marketing Category: NDA
Start Marketing Date: 20020425

Package Information of Benicar

Package NDC: 63629-3390-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-3390-1)

NDC Information of Benicar

NDC Code 63629-3390-1
Proprietary Name Benicar
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-3390-1)
Product NDC 63629-3390
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 Bryant Ranch Prepack
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