Fluorescein Sodium and Benoxinate Hydrochloride (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the Fluorescein Sodium and Benoxinate Hydrochloride drug offered from Bausch & Lomb Incorporated. 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: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: Fluorescein Sodium and Benoxinate Hydrochloride
SUBSTANCE NAME: BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Diagnostic Dye [EPC],Dyes [MoA]
ROUTE: OPHTHALMIC
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 1995-01-01
END MARKETING DATE: 0000-00-00


Fluorescein Sodium and Benoxinate Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionFluorescein Sodium and Benoxinate Hydrochloride from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 4; 2.5(mg/mL; mg/mL)
START MARKETING DATE: 1995-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-732_71938df7-eb38-4a21-9267-ea4b355b8c1e
PRODUCT NDC: 24208-732
APPLICATION NUMBER:

Other BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Altaire Pharmaceuticals Inc.ALTAFLUOR
Bausch & Lomb IncorporatedFluorescein Sodium and Benoxinate Hydrochloride