Luzu (Valeant Pharmaceuticals North America LLC)


Welcome to the PulseAid listing for the Luzu drug offered from Valeant Pharmaceuticals North America LLC. This Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Cytochrome P450 2C19 Inhibitors [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: Valeant Pharmaceuticals North America LLC
NON-PROPRIETARY NAME: LULICONAZOLE
SUBSTANCE NAME: LULICONAZOLE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Cytochrome P450 2C19 Inhibitors [MoA]
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2013-11-14
END MARKETING DATE: 0000-00-00


Luzu HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLuzu from Valeant Pharmaceuticals North America LLC
LABELER NAME: Valeant Pharmaceuticals North America LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/g)
START MARKETING DATE: 2013-11-14
END MARKETING DATE: 0000-00-00
PRODUCT ID: 99207-850_4fa7e444-9f5d-4174-b9d6-853fa6b0d860
PRODUCT NDC: 99207-850
APPLICATION NUMBER: NDA204153

Other LULICONAZOLE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Valeant Pharmaceuticals North America LLCLuzu