XILAPAK (SOLUTECH PHARMACEUTICALS LLC)
Welcome to the PulseAid listing for the XILAPAK drug offered from SOLUTECH PHARMACEUTICALS LLC. 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: | SOLUTECH PHARMACEUTICALS LLC |
NON-PROPRIETARY NAME: | FLUOCINOLONE ACETONIDE |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
START MARKETING DATE: | 2017-11-01 |
END MARKETING DATE: | 0000-00-00 |
XILAPAK HUMAN PRESCRIPTION DRUG Details:
Item Description | XILAPAK from SOLUTECH PHARMACEUTICALS LLC |
LABELER NAME: | SOLUTECH PHARMACEUTICALS LLC |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2017-11-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 70350-5218_1bdd2cf2-169b-4e44-a01b-122ee5661ae8 |
PRODUCT NDC: | 70350-5218 |
APPLICATION NUMBER: | NDA015296 |