BERBERIS QUARTZ (URIEL PHARMACY INC.)


Welcome to the PulseAid listing for the BERBERIS QUARTZ drug offered from URIEL PHARMACY 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: URIEL PHARMACY INC.
NON-PROPRIETARY NAME: BERBERIS QUARTZ
SUBSTANCE NAME: BERBERIS VULGARIS ROOT BARK; BOS TAURUS NASAL MUCOSA; SILICON DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


BERBERIS QUARTZ HUMAN OTC DRUG Details:

Item DescriptionBERBERIS QUARTZ from URIEL PHARMACY INC.
LABELER NAME: URIEL PHARMACY INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 7; 20([hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-2055_575847db-59fb-56b1-e053-2991aa0ad814
PRODUCT NDC: 48951-2055
APPLICATION NUMBER:

Other BERBERIS VULGARIS ROOT BARK; BOS TAURUS NASAL MUCOSA; SILICON DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Berberis Quartz
URIEL PHARMACY INC.BERBERIS QUARTZ