Ellzia Pak (PureTek Corporation)
Welcome to the PulseAid listing for the Ellzia Pak 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: | 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 |
Ellzia Pak HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ellzia Pak from PureTek Corporation |
| LABELER NAME: | PureTek Corporation |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2016-12-29 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 59088-846_0a7bb8c2-ecb5-4a80-9993-2c73d66b4e8d |
| PRODUCT NDC: | 59088-846 |
| APPLICATION NUMBER: | ANDA205373 |