Berberis Larix (Uriel Pharmacy Inc)


Welcome to the PulseAid listing for the Berberis Larix 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 Larix
SUBSTANCE NAME: ACHILLEA MILLEFOLIUM; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; LYTTA VESICATORIA; APIS MELLIFERA; LARIX DECIDUA RESIN
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 Larix HUMAN OTC DRUG Details:

Item DescriptionBerberis Larix from Uriel Pharmacy Inc
LABELER NAME: Uriel Pharmacy Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 3; 3; 6; 8; 8([hp_X]/1; [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: 48951-2119_54c4f177-a77d-5dfa-e054-00144ff88e88
PRODUCT NDC: 48951-2119
APPLICATION NUMBER:

Other ACHILLEA MILLEFOLIUM; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; LYTTA VESICATORIA; APIS MELLIFERA; LARIX DECIDUA RESIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy IncBerberis Larix