POTIGA (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the POTIGA drug offered from GlaxoSmithKline LLC. This Potassium Channel Openers [MoA],Potassium Channel Opener [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: GlaxoSmithKline LLC
NON-PROPRIETARY NAME: ezogabine
SUBSTANCE NAME: EZOGABINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Potassium Channel Openers [MoA],Potassium Channel Opener [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET, FILM COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2012-04-19
END MARKETING DATE: 2019-07-31


POTIGA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPOTIGA from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE: CV
ACTIVE STRENGTH: 50(mg/1)
START MARKETING DATE: 2012-04-19
END MARKETING DATE: 2019-07-31
PRODUCT ID: 0173-0810_efb88eb8-a497-4139-bc4f-865fd499d88d
PRODUCT NDC: 0173-0810
APPLICATION NUMBER: NDA022345

Other EZOGABINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCPOTIGA