NOXIPAK (SOLUTECH PHARMACEUTICALS LLC)
Welcome to the PulseAid listing for the NOXIPAK 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 and UREA |
| 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 |
NOXIPAK HUMAN PRESCRIPTION DRUG Details:
| Item Description | NOXIPAK 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: | 70350-5201_e8816c67-a9d7-4953-99e5-c2095aa10713 |
| PRODUCT NDC: | 70350-5201 |
| APPLICATION NUMBER: | NDA015296 |