Choletec (Bracco Diagnostics Inc)


Welcome to the PulseAid listing for the Choletec drug offered from Bracco Diagnostics 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: Bracco Diagnostics Inc
NON-PROPRIETARY NAME: Mebrofenin
SUBSTANCE NAME: MEBROFENIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: INTRAVENOUS
DOSAGE FORM: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1987-01-21
END MARKETING DATE: 0000-00-00


Choletec HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCholetec from Bracco Diagnostics Inc
LABELER NAME: Bracco Diagnostics Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 45(mg/1)
START MARKETING DATE: 1987-01-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0270-0083_12f4df45-879f-36f4-ded6-16857c1f20b9
PRODUCT NDC: 0270-0083
APPLICATION NUMBER: NDA018963

Other MEBROFENIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
AnazaoHealth CorporationMebrofenin
Bracco Diagnostics IncCholetec
Pharmalucence, Inc.Kit for the Preparation of Technetium Tc 99m Mebrofenin