DermacinRx PureFolix (PureTek Corporation)
Welcome to the PulseAid listing for the DermacinRx PureFolix drug offered from PureTek Corporation. This Vitamin D [Chemical/Ingredient],Vitamin D [EPC] 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: | Folic Acid, Vitamin D3 |
| SUBSTANCE NAME: | FOLIC ACID; VITAMIN D |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2015-11-03 |
| END MARKETING DATE: | 0000-00-00 |
DermacinRx PureFolix HUMAN PRESCRIPTION DRUG Details:
| Item Description | DermacinRx PureFolix from PureTek Corporation |
| LABELER NAME: | PureTek Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1; 125(mg/1; ug/1) |
| START MARKETING DATE: | 2015-11-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 59088-090_23acb62e-2a2d-5a47-e054-00144ff88e88 |
| PRODUCT NDC: | 59088-090 |
| APPLICATION NUMBER: | |
Other FOLIC ACID; VITAMIN D Pharmaceutical Manufacturers / Labelers:
