FLURESS (Akorn, Inc.)
Welcome to the PulseAid listing for the FLURESS drug offered from Akorn, 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: | Akorn, Inc. |
| NON-PROPRIETARY NAME: | Fluorescein Sodium and Benoxinate Hydrochloride |
| SUBSTANCE NAME: | FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE |
| 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: | 1995-02-01 |
| END MARKETING DATE: | 0000-00-00 |
FLURESS HUMAN PRESCRIPTION DRUG Details:
| Item Description | FLURESS from Akorn, Inc. |
| LABELER NAME: | Akorn, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2.5; 4(mg/mL; mg/mL) |
| START MARKETING DATE: | 1995-02-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 17478-640_b63db481-5b90-4817-b2f9-940ba2473d0b |
| PRODUCT NDC: | 17478-640 |
| APPLICATION NUMBER: | |
Other FLUORESCEIN SODIUM; BENOXINATE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
