Monurol (Forest Laboratories)


Welcome to the PulseAid listing for the Monurol drug offered from Forest Laboratories. 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: Forest Laboratories
NON-PROPRIETARY NAME: Fosfomycin tromethamine
SUBSTANCE NAME: FOSFOMYCIN TROMETHAMINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: POWDER
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1996-12-19
END MARKETING DATE: 0000-00-00


Monurol HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMonurol from Forest Laboratories
LABELER NAME: Forest Laboratories
DEA SCHEDULE:
ACTIVE STRENGTH: 3(g/1)
START MARKETING DATE: 1996-12-19
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0456-4300_061b7b01-ac4c-43fc-b487-8c01d0cfb51e
PRODUCT NDC: 0456-4300
APPLICATION NUMBER: NDA050717

Other FOSFOMYCIN TROMETHAMINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Forest LaboratoriesMonurol