Neurovita (RUBIMED AG)


Welcome to the PulseAid listing for the Neurovita 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: MELISSA OFFICINALIS, SUS SCROFA CEREBELLUM, AMBERGRIS, CINCHONA OFFICINALIS BARK, CUPRIC ACETATE, and PHOSPHORUS
SUBSTANCE NAME: MELISSA OFFICINALIS; SUS SCROFA CEREBELLUM; AMBERGRIS; CINCHONA OFFICINALIS BARK; CUPRIC ACETATE; PHOSPHORUS
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


Neurovita HUMAN OTC DRUG Details:

Item DescriptionNeurovita from RUBIMED AG
LABELER NAME: RUBIMED AG
DEA SCHEDULE:
ACTIVE STRENGTH: 4; 21; 21; 50; 200; 12([hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_M]/mL)
START MARKETING DATE: 2015-05-07
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66343-003_fa5f780f-fb66-404e-820b-4588a7a8e81f
PRODUCT NDC: 66343-003
APPLICATION NUMBER:

Other MELISSA OFFICINALIS; SUS SCROFA CEREBELLUM; AMBERGRIS; CINCHONA OFFICINALIS BARK; CUPRIC ACETATE; PHOSPHORUS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
RUBIMED AGNeurovita