Dofetilide (Greenstone LLC)


Welcome to the PulseAid listing for the Dofetilide drug offered from Greenstone LLC. This Antiarrhythmic [EPC] 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: Greenstone LLC
NON-PROPRIETARY NAME: dofetilide
SUBSTANCE NAME: DOFETILIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antiarrhythmic [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-05-01
END MARKETING DATE: 0000-00-00


Dofetilide HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDofetilide from Greenstone LLC
LABELER NAME: Greenstone LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 0.125(mg/1)
START MARKETING DATE: 2016-05-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59762-0037_0f7c3696-cc1c-413e-bb30-9f18abb27fa1
PRODUCT NDC: 59762-0037
APPLICATION NUMBER: NDA020931

Other DOFETILIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Avera McKennan HospitalTikosyn
Greenstone LLCDofetilide
Mayne Pharma Inc.Dofetilide
Pfizer Laboratories Div Pfizer IncTikosyn