Lachesis (Energique, Inc.)
Welcome to the PulseAid listing for the Lachesis 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: | Lachesis Mutus |
SUBSTANCE NAME: | LACHESIS MUTA VENOM |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | LIQUID |
MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
START MARKETING DATE: | 2016-08-22 |
END MARKETING DATE: | 0000-00-00 |
Lachesis HUMAN OTC DRUG Details:
Item Description | Lachesis from Energique, Inc. |
LABELER NAME: | Energique, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 200([hp_C]/mL) |
START MARKETING DATE: | 2016-08-22 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 44911-0388_ea14b75d-4c77-4dee-a8bd-ef4fecb6e8f6 |
PRODUCT NDC: | 44911-0388 |
APPLICATION NUMBER: | |
Other LACHESIS MUTA VENOM Pharmaceutical Manufacturers / Labelers: