# AK-FLUOR

NDC: 81298-8660
Generic name: fluorescein
Labeler / Manufacturer: Long Grove Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20240928

FDA application: NDA022186

## Active ingredients

- FLUORESCEIN SODIUM: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81298-8660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81298-8660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=73511e79-c050-4dc0-aa2f-a79ed320b5b0
