Berberis Pyrite (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Berberis Pyrite 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 Pyrite
SUBSTANCE NAME: APIS MELLIFERA; BERBERIS VULGARIS ROOT BARK; FERROUS DISULFIDE; SAGE; MERCURIC SULFIDE
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 Pyrite HUMAN OTC DRUG Details:

Item DescriptionBerberis Pyrite from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 3; 3; 3; 20([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-2053_575847db-59bb-56b1-e053-2991aa0ad814
PRODUCT NDC: 48951-2053
APPLICATION NUMBER:

Other APIS MELLIFERA; BERBERIS VULGARIS ROOT BARK; FERROUS DISULFIDE; SAGE; MERCURIC SULFIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Berberis Pyrite