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 Description | RIDAURA from Prometheus Laboratories Inc. |
LABELER NAME: | Prometheus Laboratories Inc. |
DEA SCHEDULE: |
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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: