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 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 Description | FLUORESCITE from Alcon, Inc. |
LABELER NAME: | Alcon, Inc. |
DEA SCHEDULE: |
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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: