Polibar ACB (E-Z-EM Canada Inc)


Welcome to the PulseAid listing for the Polibar ACB drug offered from E-Z-EM Canada 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: E-Z-EM Canada Inc
NON-PROPRIETARY NAME: BARIUM SULFATE
SUBSTANCE NAME: BARIUM SULFATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: RECTAL
DOSAGE FORM: POWDER, FOR SUSPENSION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 1978-04-15
END MARKETING DATE: 0000-00-00


Polibar ACB HUMAN PRESCRIPTION DRUG Details:

Item DescriptionPolibar ACB from E-Z-EM Canada Inc
LABELER NAME: E-Z-EM Canada Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 965(mg/g)
START MARKETING DATE: 1978-04-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 32909-804_330cbb50-50ca-4251-b9c7-14e5fa89f7a8
PRODUCT NDC: 32909-804
APPLICATION NUMBER:

Other BARIUM SULFATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
E-Z-EM Canada IncVaribar Thin Liquid
E-Z-EM, INC.E-Z-Disk
Genus Medical Technologies, LLCVanilla SilQ