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 Description | Fluorescein Sodium and Benoxinate Hydrochloride from Bausch & Lomb Incorporated |
LABELER NAME: | Bausch & Lomb Incorporated |
DEA SCHEDULE: |
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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: