Ambrosia artemisiaefolia (Laboratoires Boiron)
Welcome to the PulseAid listing for the Ambrosia artemisiaefolia drug offered from Laboratoires Boiron. 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: | Laboratoires Boiron |
NON-PROPRIETARY NAME: | AMBROSIA ARTEMISIIFOLIA |
SUBSTANCE NAME: | AMBROSIA ARTEMISIIFOLIA |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | PELLET |
MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
START MARKETING DATE: | 1983-03-03 |
END MARKETING DATE: | 0000-00-00 |
Ambrosia artemisiaefolia HUMAN OTC DRUG Details:
Item Description | Ambrosia artemisiaefolia from Laboratoires Boiron |
LABELER NAME: | Laboratoires Boiron |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 6([hp_X]/1) |
START MARKETING DATE: | 1983-03-03 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0220-0225_4165c980-7c4b-11e6-81e7-424c58303031 |
PRODUCT NDC: | 0220-0225 |
APPLICATION NUMBER: | |
Other AMBROSIA ARTEMISIIFOLIA Pharmaceutical Manufacturers / Labelers: