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: |
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| 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:
