EUPATORIUM PERFOLIATUM (HOMEOLAB USA INC.)
Welcome to the PulseAid listing for the EUPATORIUM PERFOLIATUM drug offered from HOMEOLAB USA 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: | HOMEOLAB USA INC. |
NON-PROPRIETARY NAME: | EUPATORIUM PERFOLIATUM |
SUBSTANCE NAME: | EUPATORIUM PERFOLIATUM FLOWERING TOP |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | PELLET |
MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
START MARKETING DATE: | 2013-11-18 |
END MARKETING DATE: | 0000-00-00 |
EUPATORIUM PERFOLIATUM HUMAN OTC DRUG Details:
Item Description | EUPATORIUM PERFOLIATUM from HOMEOLAB USA INC. |
LABELER NAME: | HOMEOLAB USA INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 1([hp_X]/1) |
START MARKETING DATE: | 2013-11-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 60512-1017_aeb4b3a7-164a-4862-83dd-be2aa0d067c0 |
PRODUCT NDC: | 60512-1017 |
APPLICATION NUMBER: | |
Other EUPATORIUM PERFOLIATUM FLOWERING TOP Pharmaceutical Manufacturers / Labelers: