Borrelia burgdorferi (Newton Laboratories, Inc.)


Welcome to the PulseAid listing for the Borrelia burgdorferi drug offered from Newton Laboratories, Inc.. This pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Newton Laboratories, Inc.
NON-PROPRIETARY NAME: Borrelia burgdorferi
SUBSTANCE NAME: BORRELIA BURGDORFERI
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2011-09-01
END MARKETING DATE: 0000-00-00


Borrelia burgdorferi HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBorrelia burgdorferi from Newton Laboratories, Inc.
LABELER NAME: Newton Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 200([hp_C]/mL)
START MARKETING DATE: 2011-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 55714-6083_ec0dda76-af8a-252f-eee8-91753ef2144e
PRODUCT NDC: 55714-6083
APPLICATION NUMBER:

Other BORRELIA BURGDORFERI Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Deseret Biologicals, Inc.Borrelia Remedy
Newton Laboratories, Inc.Borrelia burgdorferi