# Ketotifen Fumarate

NDC: 68788-8715
Generic name: Ketotifen Fumarate
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20240712

FDA application: ANDA204059

## 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:"68788-8715"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8715
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5196ec5b-42d9-40db-a77a-c00360b8cee6