E-Z-Cat Dry (E-Z-EM Canada Inc)


Welcome to the PulseAid listing for the E-Z-Cat Dry drug offered from E-Z-EM Canada Inc. This Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] 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: Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
ROUTE: ORAL
DOSAGE FORM: POWDER, FOR SUSPENSION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-09-28
END MARKETING DATE: 0000-00-00


E-Z-Cat Dry HUMAN PRESCRIPTION DRUG Details:

Item DescriptionE-Z-Cat Dry from E-Z-EM Canada Inc
LABELER NAME: E-Z-EM Canada Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 400(mg/g)
START MARKETING DATE: 2017-09-28
END MARKETING DATE: 0000-00-00
PRODUCT ID: 32909-717_1c8fb588-e29e-4897-a22f-95e16e9bb6cc
PRODUCT NDC: 32909-717
APPLICATION NUMBER: NDA208036

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