# Ketotifen Fumarate Ophthalmic Solution

NDC: 68788-4084
Generic name: Ketotifen Fumarate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20260227

FDA application: ANDA077958

## Active ingredients

- KETOTIFEN FUMARATE: .25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-4084"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-4084
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f4dd2b53-c2f2-4c5a-8eb0-c96d79cf419c