RIDAURA (Prometheus Laboratories Inc.)


Welcome to the PulseAid listing for the RIDAURA drug offered from Prometheus Laboratories 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: Prometheus Laboratories 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: 1985-04-24
END MARKETING DATE: 0000-00-00


RIDAURA HUMAN PRESCRIPTION DRUG Details:

Item DescriptionRIDAURA from Prometheus Laboratories Inc.
LABELER NAME: Prometheus Laboratories Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3(mg/1)
START MARKETING DATE: 1985-04-24
END MARKETING DATE: 0000-00-00
PRODUCT ID: 65483-093_6008addc-7f8e-45bb-8aec-54dd54a788ac
PRODUCT NDC: 65483-093
APPLICATION NUMBER: NDA018689

Other AURANOFIN Pharmaceutical Manufacturers / Labelers:

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