Dry Eye Test (Nomax Inc.)


Welcome to the PulseAid listing for the Dry Eye Test drug offered from Nomax Inc.. This Diagnostic Dye [EPC],Dyes [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view the 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: Nomax Inc.
NON-PROPRIETARY NAME: Fluorescein Sodium
SUBSTANCE NAME: FLUORESCEIN SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Diagnostic Dye [EPC],Dyes [MoA]
ROUTE: OPHTHALMIC
DOSAGE FORM: STRIP
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2013-12-05
END MARKETING DATE: 0000-00-00


Dry Eye Test HUMAN PRESCRIPTION DRUG Details:

Item DescriptionDry Eye Test from Nomax Inc.
LABELER NAME: Nomax Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.12(mg/1)
START MARKETING DATE: 2013-12-05
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51801-008_08dd04c1-ca76-4b5d-ae29-1479238743b2
PRODUCT NDC: 51801-008
APPLICATION NUMBER:

Other FLUORESCEIN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
AkornAK-FLUOR
Alcon, Inc.FLUORESCITE
HUB Pharmaceuticals, Inc.BioGlo
Nomax Inc.GloStrips
REMEDYREPACK INC.BioGlo