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:
