DERMAWERX ZMT PAK (Patchwerx Labs, Inc.)
Welcome to the PulseAid listing for the DERMAWERX ZMT PAK drug offered from Patchwerx Labs, Inc.. 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: | Patchwerx Labs, Inc. |
NON-PROPRIETARY NAME: | ZINC OXIDE, MENTHOL, UNSPECIFIED FORM, and TRETINOIN |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2015-09-08 |
END MARKETING DATE: | 0000-00-00 |
DERMAWERX ZMT PAK HUMAN PRESCRIPTION DRUG Details:
Item Description | DERMAWERX ZMT PAK from Patchwerx Labs, Inc. |
LABELER NAME: | Patchwerx Labs, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2015-09-08 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69329-600_2468bf3e-e346-1d73-e054-00144ff8d46c |
PRODUCT NDC: | 69329-600 |
APPLICATION NUMBER: | ANDA075264 |