edarbi - 64764-884-90 - (Azilsartan kamedoxomil)

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Drug Information of edarbi

Product NDC: 64764-884
Proprietary Name: edarbi
Non Proprietary Name: Azilsartan kamedoxomil
Active Ingredient(s): 80    mg/1 & nbsp;   Azilsartan kamedoxomil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of edarbi

Product NDC: 64764-884
Labeler Name: Takeda Pharmaceuticals America, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA200796
Marketing Category: NDA
Start Marketing Date: 20110225

Package Information of edarbi

Package NDC: 64764-884-90
Package Description: 90 TABLET in 1 BOTTLE (64764-884-90)

NDC Information of edarbi

NDC Code 64764-884-90
Proprietary Name edarbi
Package Description 90 TABLET in 1 BOTTLE (64764-884-90)
Product NDC 64764-884
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Azilsartan kamedoxomil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110225
Marketing Category Name NDA
Labeler Name Takeda Pharmaceuticals America, Inc.
Substance Name AZILSARTAN KAMEDOXOMIL
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Angiotensin 2 Type 1 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Decreased Blood Pressure [PE]

Complete Information of edarbi


General Information