FUCUS VESICULOSUS (HOMEOLAB USA INC.)
Welcome to the PulseAid listing for the FUCUS VESICULOSUS 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: | FUCUS VESICULOSUS |
SUBSTANCE NAME: | FUCUS VESICULOSUS |
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 |
FUCUS VESICULOSUS HUMAN OTC DRUG Details:
Item Description | FUCUS VESICULOSUS 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: | 60512-6695_700fa09c-5049-427a-a655-a91b2281a9fd |
PRODUCT NDC: | 60512-6695 |
APPLICATION NUMBER: | |
Other FUCUS VESICULOSUS Pharmaceutical Manufacturers / Labelers: