Berberis Populus (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Berberis Populus 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 Populus
SUBSTANCE NAME: BERBERIS VULGARIS ROOT BARK; POPULUS TREMULA WHOLE; SAW PALMETTO; URTICA URENS; LARIX DECIDUA RESIN; BLACK PEPPER
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


Berberis Populus HUMAN OTC DRUG Details:

Item DescriptionBerberis Populus from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 2; 3; 3; 3; 8; 17([hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-2047_83b516de-d480-4f2d-98b3-ae85ab6a5070
PRODUCT NDC: 48951-2047
APPLICATION NUMBER:

Other BERBERIS VULGARIS ROOT BARK; POPULUS TREMULA WHOLE; SAW PALMETTO; URTICA URENS; LARIX DECIDUA RESIN; BLACK PEPPER Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Berberis Populus