PREGNENOLONE (Energique, Inc.)


Welcome to the PulseAid listing for the PREGNENOLONE drug offered from Energique, Inc.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Energique, Inc.
NON-PROPRIETARY NAME: Pregnenolone
SUBSTANCE NAME: PREGNENOLONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2015-07-09
END MARKETING DATE: 0000-00-00


PREGNENOLONE HUMAN OTC DRUG Details:

Item DescriptionPREGNENOLONE from Energique, Inc.
LABELER NAME: Energique, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 30([hp_C]/mL)
START MARKETING DATE: 2015-07-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 44911-0201_61474eea-743e-481b-b379-517e4ff5214b
PRODUCT NDC: 44911-0201
APPLICATION NUMBER:

Other PREGNENOLONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Energique, Inc.PREGNENOLONE