Betula Argentum (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Betula Argentum 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: Betula Argentum
SUBSTANCE NAME: BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; APIS MELLIFERA; FORMICA RUFA; SILVER; ARNICA MONTANA
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


Betula Argentum HUMAN OTC DRUG Details:

Item DescriptionBetula Argentum from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 1; 6; 7; 8; 17([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: 48951-2064_5758d564-28ed-cdbd-e053-2991aa0a8a42
PRODUCT NDC: 48951-2064
APPLICATION NUMBER:

Other BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; APIS MELLIFERA; FORMICA RUFA; SILVER; ARNICA MONTANA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Betula Argentum