RIDAURA (Sebela Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the RIDAURA drug offered from Sebela Pharmaceuticals Inc.. This 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: Sebela Pharmaceuticals Inc.
NON-PROPRIETARY NAME: auranofin
SUBSTANCE NAME: AURANOFIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-12-15
END MARKETING DATE: 0000-00-00


RIDAURA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionRIDAURA from Sebela Pharmaceuticals Inc.
LABELER NAME: Sebela Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3(mg/1)
START MARKETING DATE: 2016-12-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54766-093_43ba3de1-ab2f-06f6-e054-00144ff8d46c
PRODUCT NDC: 54766-093
APPLICATION NUMBER: NDA018689

Other AURANOFIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Prometheus Laboratories Inc.RIDAURA
Sebela Pharmaceuticals Inc.RIDAURA