Oxalis e pl. tota 3 (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Oxalis e pl. tota 3 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: Oxalis e pl. tota 3
SUBSTANCE NAME: OXALIS MONTANA LEAF
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


Oxalis e pl. tota 3 HUMAN OTC DRUG Details:

Item DescriptionOxalis e pl. tota 3 from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3([hp_X]/mL)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-7109_b8ae6ff2-f300-4240-9515-539528d818b9
PRODUCT NDC: 48951-7109
APPLICATION NUMBER:

Other OXALIS MONTANA LEAF Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Oxalis 10