FLUORESCITE (Alcon, Inc.)


Welcome to the PulseAid listing for the FLUORESCITE drug offered from Alcon, 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: Alcon, 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: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1972-09-15
END MARKETING DATE: 0000-00-00


FLUORESCITE HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFLUORESCITE from Alcon, Inc.
LABELER NAME: Alcon, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/mL)
START MARKETING DATE: 1972-09-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0065-0092_b82faeaa-c290-5170-bc7a-fe7144b76cd2
PRODUCT NDC: 0065-0092
APPLICATION NUMBER: NDA021980

Other FLUORESCEIN SODIUM Pharmaceutical Manufacturers / Labelers:

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