E-Z-HD (E-Z-EM Canada Inc)
Welcome to the PulseAid listing for the E-Z-HD 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: | 2016-01-11 |
END MARKETING DATE: | 0000-00-00 |
E-Z-HD HUMAN PRESCRIPTION DRUG Details:
Item Description | E-Z-HD from E-Z-EM Canada Inc |
LABELER NAME: | E-Z-EM Canada Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 980(mg/g) |
START MARKETING DATE: | 2016-01-11 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 32909-764_6b8b46a8-33bc-950a-e678-3abf8642ed57 |
PRODUCT NDC: | 32909-764 |
APPLICATION NUMBER: | NDA208036 |
Other BARIUM SULFATE Pharmaceutical Manufacturers / Labelers: