Flurox (OCuSOFT, Inc.)


Welcome to the PulseAid listing for the Flurox drug offered from OCuSOFT, Inc.. This Diagnostic Dye [EPC],Dyes [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: OCuSOFT, Inc.
NON-PROPRIETARY NAME: Fluorescein Sodium 2.5mg (0.25%), Benoxinate Hydrochloride 4mg (0.4%)
SUBSTANCE NAME: FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Diagnostic Dye [EPC],Dyes [MoA]
ROUTE: OPHTHALMIC
DOSAGE FORM: SOLUTION
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2014-01-29
END MARKETING DATE: 0000-00-00


Flurox HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFlurox from OCuSOFT, Inc.
LABELER NAME: OCuSOFT, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 2.5; 4(mg/mL; mg/mL)
START MARKETING DATE: 2014-01-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54799-508_5476a07b-4f5c-3b6b-38b3-b006435306c1
PRODUCT NDC: 54799-508
APPLICATION NUMBER:

Other FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Akorn, Inc.FLURESS
OCuSOFT, Inc.Flurox