Aconite (Energique, Inc.)
Welcome to the PulseAid listing for the Aconite 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: | Aconitum Napellus |
SUBSTANCE NAME: | ACONITUM NAPELLUS |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
START MARKETING DATE: | 2015-05-14 |
END MARKETING DATE: | 0000-00-00 |
Aconite HUMAN OTC DRUG Details:
Item Description | Aconite from Energique, Inc. |
LABELER NAME: | Energique, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 30([hp_C]/mL) |
START MARKETING DATE: | 2015-05-14 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 44911-0152_9788ac4b-7443-4846-822c-9f09da9bb31d |
PRODUCT NDC: | 44911-0152 |
APPLICATION NUMBER: | |
Other ACONITUM NAPELLUS Pharmaceutical Manufacturers / Labelers: