Leximenth (PureTek Corporation)
Welcome to the PulseAid listing for the Leximenth drug offered from PureTek Corporation. 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: | PureTek Corporation |
| NON-PROPRIETARY NAME: | diclofenac sodium, lidocaine, menthol |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2017-10-30 |
| END MARKETING DATE: | 0000-00-00 |
Leximenth HUMAN PRESCRIPTION DRUG Details:
| Item Description | Leximenth from PureTek Corporation |
| LABELER NAME: | PureTek Corporation |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2017-10-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 59088-704_04d0f334-9ffa-4141-b567-97acb1bf642f |
| PRODUCT NDC: | 59088-704 |
| APPLICATION NUMBER: | ANDA202769 |