Yaliira Pak (Shoreline Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Yaliira Pak 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: | triamcinolone acetonide, dimethicone |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-12-29 |
| END MARKETING DATE: | 0000-00-00 |
Yaliira Pak HUMAN PRESCRIPTION DRUG Details:
| Item Description | Yaliira Pak from Shoreline Pharmaceuticals, Inc. |
| LABELER NAME: | Shoreline Pharmaceuticals, Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2016-12-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 69621-846_9db9f00e-236f-4198-882f-412c8016ad24 |
| PRODUCT NDC: | 69621-846 |
| APPLICATION NUMBER: | ANDA205373 |