Plumeria Rubra (Hahnemann Laboratories, Inc.)


Welcome to the PulseAid listing for the Plumeria Rubra 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: Plumeria Rubra
SUBSTANCE NAME: PLUMERIA RUBRA WHOLE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: BUCCAL; ORAL; SUBLINGUAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2017-05-04
END MARKETING DATE: 0000-00-00


Plumeria Rubra HUMAN OTC DRUG Details:

Item DescriptionPlumeria Rubra from Hahnemann Laboratories, Inc.
LABELER NAME: Hahnemann Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 30([hp_C]/[hp_C])
START MARKETING DATE: 2017-05-04
END MARKETING DATE: 0000-00-00
PRODUCT ID: 63545-686_4ebaa367-2c67-431b-e054-00144ff88e88
PRODUCT NDC: 63545-686
APPLICATION NUMBER:

Other PLUMERIA RUBRA WHOLE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hahnemann Laboratories, Inc.Plumeria Rubra