# KETOTIFEN FUMARATE

NDC: 76385-106
Generic name: KETOTIFEN FUMARATE
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: OPHTHALMIC
Marketing started: 20211015

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:"76385-106"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76385-106
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0fe119ad-cb44-4e90-a096-0ed0ba63dc31