Xelitral (Shoreline Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Xelitral drug offered from Shoreline Pharmaceuticals, 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: | Shoreline Pharmaceuticals, Inc. |
| NON-PROPRIETARY NAME: | diclofenac sodium, capsaicin |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-05-10 |
| END MARKETING DATE: | 0000-00-00 |
Xelitral HUMAN PRESCRIPTION DRUG Details:
| Item Description | Xelitral from Shoreline Pharmaceuticals, Inc. |
| LABELER NAME: | Shoreline Pharmaceuticals, Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2016-05-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 69621-343_4a55f7b2-dec1-416d-8fe0-ea25c1f64b30 |
| PRODUCT NDC: | 69621-343 |
| APPLICATION NUMBER: | ANDA202769 |