Zylet (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the Zylet drug offered from Bausch & Lomb Incorporated. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] 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: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: loteprednol etabonate and tobramycin
SUBSTANCE NAME: LOTEPREDNOL ETABONATE; TOBRAMYCIN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient]
ROUTE: OPHTHALMIC
DOSAGE FORM: SUSPENSION/ DROPS
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2004-12-14
END MARKETING DATE: 0000-00-00


Zylet HUMAN PRESCRIPTION DRUG Details:

Item DescriptionZylet from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 3(mg/mL; mg/mL)
START MARKETING DATE: 2004-12-14
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-358_fb4735b1-0f70-459a-a025-8fefd18ac4e4
PRODUCT NDC: 24208-358
APPLICATION NUMBER: NDA050804

Other LOTEPREDNOL ETABONATE; TOBRAMYCIN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bausch & Lomb IncorporatedZylet