Oxsoralen-Ultra (Valeant Pharmaceuticals North America LLC)
Welcome to the PulseAid listing for the Oxsoralen-Ultra drug offered from Valeant Pharmaceuticals North America LLC. This Photoabsorption [MoA],Photoactivated Radical Generator [EPC],Photosensitizing Activity [PE],Psoralen [EPC],Psoralens [Chemical/Ingredient] 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: | Valeant Pharmaceuticals North America LLC |
NON-PROPRIETARY NAME: | Methoxsalen |
SUBSTANCE NAME: | METHOXSALEN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Photoabsorption [MoA],Photoactivated Radical Generator [EPC],Photosensitizing Activity [PE],Psoralen [EPC],Psoralens [Chemical/Ingredient] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE, LIQUID FILLED |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1986-10-30 |
END MARKETING DATE: | 0000-00-00 |
Oxsoralen-Ultra HUMAN PRESCRIPTION DRUG Details:
Item Description | Oxsoralen-Ultra from Valeant Pharmaceuticals North America LLC |
LABELER NAME: | Valeant Pharmaceuticals North America LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/1) |
START MARKETING DATE: | 1986-10-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0187-0650_3882c95a-4bb1-438d-8316-06517316e351 |
PRODUCT NDC: | 0187-0650 |
APPLICATION NUMBER: | NDA019600 |
Other METHOXSALEN Pharmaceutical Manufacturers / Labelers: