edarbi (Takeda Pharmaceuticals America, Inc.)


Welcome to the PulseAid listing for the edarbi drug offered from Takeda Pharmaceuticals America, Inc.. This Angiotensin 2 Type 1 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Decreased Blood Pressure [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Takeda Pharmaceuticals America, Inc.
NON-PROPRIETARY NAME: Azilsartan kamedoxomil
SUBSTANCE NAME: AZILSARTAN KAMEDOXOMIL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Angiotensin 2 Type 1 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Decreased Blood Pressure [PE]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2011-02-25
END MARKETING DATE: 2018-02-01


edarbi HUMAN PRESCRIPTION DRUG Details:

Item Descriptionedarbi from Takeda Pharmaceuticals America, Inc.
LABELER NAME: Takeda Pharmaceuticals America, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 40(mg/1)
START MARKETING DATE: 2011-02-25
END MARKETING DATE: 2018-02-01
PRODUCT ID: 64764-844_142b45c8-d1b0-436e-9b0a-80d48e569d9f
PRODUCT NDC: 64764-844
APPLICATION NUMBER: NDA200796

Other AZILSARTAN KAMEDOXOMIL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Arbor PharmaceuticalsEdarbi
Takeda Pharmaceuticals America, Inc.edarbi