Anxiovita (RUBIMED AG)


Welcome to the PulseAid listing for the Anxiovita drug offered from RUBIMED AG. 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: RUBIMED AG
NON-PROPRIETARY NAME: PIPER METHYSTICUM ROOT, HYPERICUM PERFORATUM, SUS SCROFA CEREBELLUM, and ACONITUM NAPELLUS
SUBSTANCE NAME: PIPER METHYSTICUM ROOT; HYPERICUM PERFORATUM; SUS SCROFA CEREBELLUM; ACONITUM NAPELLUS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2015-05-07
END MARKETING DATE: 0000-00-00


Anxiovita HUMAN OTC DRUG Details:

Item DescriptionAnxiovita from RUBIMED AG
LABELER NAME: RUBIMED AG
DEA SCHEDULE:
ACTIVE STRENGTH: 12; 21; 200; 18([hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_M]/mL)
START MARKETING DATE: 2015-05-07
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66343-001_57004a41-dd28-40fd-a0a0-9a50bde92032
PRODUCT NDC: 66343-001
APPLICATION NUMBER:

Other PIPER METHYSTICUM ROOT; HYPERICUM PERFORATUM; SUS SCROFA CEREBELLUM; ACONITUM NAPELLUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
RUBIMED AGAnxiovita