# FML

NDC: 0781-6187
Generic name: fluorometholone
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20260330

FDA application: ANDA218819

## Active ingredients

- FLUOROMETHOLONE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-6187"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-6187
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c9cbf06e-5413-4c3c-9ded-174c856a4ce1