ALREX (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the ALREX drug offered from Bausch & Lomb Incorporated. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [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: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: loteprednol etabonate
SUBSTANCE NAME: LOTEPREDNOL ETABONATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: OPHTHALMIC
DOSAGE FORM: SUSPENSION/ DROPS
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1998-03-09
END MARKETING DATE: 0000-00-00


ALREX HUMAN PRESCRIPTION DRUG Details:

Item DescriptionALREX from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 2(mg/mL)
START MARKETING DATE: 1998-03-09
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-353_57c78944-babf-4e15-a3d9-b02bcd95ddae
PRODUCT NDC: 24208-353
APPLICATION NUMBER: NDA020803

Other LOTEPREDNOL ETABONATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bausch & Lomb IncorporatedLOTEMAX
Physicians Total Care, Inc.ALREX
STAT Rx USA LLCALREX