Quercus Rubra Glandium (Hahnemann Laboratories, Inc.)


Welcome to the PulseAid listing for the Quercus Rubra Glandium drug offered from Hahnemann Laboratories, 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: Hahnemann Laboratories, Inc.
NON-PROPRIETARY NAME: Quercus Rubra Glandium
SUBSTANCE NAME: QUERCUS RUBRA WHOLE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: BUCCAL; ORAL; SUBLINGUAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2016-12-01
END MARKETING DATE: 0000-00-00


Quercus Rubra Glandium HUMAN OTC DRUG Details:

Item DescriptionQuercus Rubra Glandium from Hahnemann Laboratories, Inc.
LABELER NAME: Hahnemann Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 30([hp_C]/[hp_C])
START MARKETING DATE: 2016-12-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63545-666_44bdd485-709d-28a1-e054-00144ff88e88
PRODUCT NDC: 63545-666
APPLICATION NUMBER:

Other QUERCUS RUBRA WHOLE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hahnemann Laboratories, Inc.Quercus Rubra Glandium