Psorizide Ultra (PLYMOUTH HEALTHCARE PRODUCTS LLC)


Welcome to the PulseAid listing for the Psorizide Ultra drug offered from PLYMOUTH HEALTHCARE PRODUCTS LLC. This Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE] 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: PLYMOUTH HEALTHCARE PRODUCTS LLC
NON-PROPRIETARY NAME: Potassium Bromide, Nickel Sulfate, and Zinc Bromide
SUBSTANCE NAME: POTASSIUM BROMIDE; NICKEL SULFATE; ZINC BROMIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1997-10-01
END MARKETING DATE: 0000-00-00


Psorizide Ultra HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPsorizide Ultra from PLYMOUTH HEALTHCARE PRODUCTS LLC
LABELER NAME: PLYMOUTH HEALTHCARE PRODUCTS LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 1; 4([hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 1997-10-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 61480-124_3ed2138f-db38-4878-92b8-97b6d78f98e1
PRODUCT NDC: 61480-124
APPLICATION NUMBER:

Other POTASSIUM BROMIDE; NICKEL SULFATE; ZINC BROMIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
PLYMOUTH HEALTHCARE PRODUCTS LLCPsorizide Ultra