DermacinRx FoliPlus D (PureTek Corporation)


Welcome to the PulseAid listing for the DermacinRx FoliPlus D 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: CAPSULE, LIQUID FILLED
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2016-07-15
END MARKETING DATE: 0000-00-00


DermacinRx FoliPlus D HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDermacinRx FoliPlus D from PureTek Corporation
LABELER NAME: PureTek Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 83.325(mg/1; ug/1)
START MARKETING DATE: 2016-07-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59088-128_37b19575-02b8-25b6-e054-00144ff8d46c
PRODUCT NDC: 59088-128
APPLICATION NUMBER:

Other FOLIC ACID; VITAMIN D Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
PureTek CorporationDermacinRx PureFolix
Shoreline Pharmaceuticals, Inc.Folixapure
SolubiomixOrtho D