DUREZOL (Alcon Laboratories, Inc.)


Welcome to the PulseAid listing for the DUREZOL drug offered from Alcon Laboratories, 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: Alcon Laboratories, Inc.
NON-PROPRIETARY NAME: DUREZOL
SUBSTANCE NAME: DIFLUPREDNATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: OPHTHALMIC
DOSAGE FORM: EMULSION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2011-01-25
END MARKETING DATE: 0000-00-00


DUREZOL HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDUREZOL from Alcon Laboratories, Inc.
LABELER NAME: Alcon Laboratories, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.5(mg/mL)
START MARKETING DATE: 2011-01-25
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0065-9240_55ac2531-fed8-4f32-9323-5adb6b378dc8
PRODUCT NDC: 0065-9240
APPLICATION NUMBER: NDA022212

Other DIFLUPREDNATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Alcon Laboratories, Inc.DUREZOL
Physicians Total Care, Inc.DUREZOL