Eczemol (PLYMOUTH HEALTHCARE PRODUCTS LLC)


Welcome to the PulseAid listing for the Eczemol drug offered from PLYMOUTH HEALTHCARE PRODUCTS LLC. 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: PLYMOUTH HEALTHCARE PRODUCTS LLC
NON-PROPRIETARY NAME: Potassium Bromide, Nickel Sulfate, and Sulfur
SUBSTANCE NAME: POTASSIUM BROMIDE; NICKEL SULFATE; SULFUR
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2001-11-15
END MARKETING DATE: 0000-00-00


Eczemol HUMAN PRESCRIPTION DRUG Details:

Item DescriptionEczemol from PLYMOUTH HEALTHCARE PRODUCTS LLC
LABELER NAME: PLYMOUTH HEALTHCARE PRODUCTS LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 1; 1([hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2001-11-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 61480-127_d8564f2e-5e43-45d9-96bd-e05196e4e891
PRODUCT NDC: 61480-127
APPLICATION NUMBER:

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

Manufacturer / LabelerProprietary Name
PLYMOUTH HEALTHCARE PRODUCTS LLCEczemol