ALTAFLUOR (Altaire Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the ALTAFLUOR drug offered from Altaire Pharmaceuticals 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: Altaire Pharmaceuticals Inc.
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
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2000-06-21
END MARKETING DATE: 0000-00-00


ALTAFLUOR HUMAN PRESCRIPTION DRUG Details:

Item DescriptionALTAFLUOR from Altaire Pharmaceuticals Inc.
LABELER NAME: Altaire Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 4; 2.5(mg/mL; mg/mL)
START MARKETING DATE: 2000-06-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59390-206_3f415ffe-f95c-418b-9ee3-a1e34670a4e5
PRODUCT NDC: 59390-206
APPLICATION NUMBER:

Other BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM Pharmaceutical Manufacturers / Labelers:

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