SORILUX (Stiefel Laboratories Inc)
Welcome to the PulseAid listing for the SORILUX drug offered from Stiefel Laboratories Inc. This Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] 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: | Stiefel Laboratories Inc |
NON-PROPRIETARY NAME: | calcipotriene |
SUBSTANCE NAME: | CALCIPOTRIENE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |
ROUTE: | TOPICAL |
DOSAGE FORM: | AEROSOL, FOAM |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2010-10-26 |
END MARKETING DATE: | 2018-10-31 |
SORILUX HUMAN PRESCRIPTION DRUG Details:
Item Description | SORILUX from Stiefel Laboratories Inc |
LABELER NAME: | Stiefel Laboratories Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50(ug/g) |
START MARKETING DATE: | 2010-10-26 |
END MARKETING DATE: | 2018-10-31 |
PRODUCT ID: | 0145-2130_8469d93a-5a7a-4c39-8127-e822642f3f58 |
PRODUCT NDC: | 0145-2130 |
APPLICATION NUMBER: | NDA022563 |
Other CALCIPOTRIENE Pharmaceutical Manufacturers / Labelers: